Advanced High School Chemistry Flashcards: Complete 9-Part Course Review

Review a rigorous nine-part high school chemistry course with 450 concise cards covering concepts, models, equations, calculation setup, and lab reasoning.

Sobre este mazo

Study advanced high school chemistry through 450 independently written English flashcards arranged as one nine-part sequence. The course moves from atomic structure and bonding to properties of substances and mixtures, reactions, kinetics, thermochemistry, equilibrium, acids and bases, thermodynamics, and electrochemistry. Prerequisites appear before dependent models and calculations.

What the cards practice

The cards practice five useful recall paths: concept to explanation; model or representation to interpretation; equation to meaning and use; short setup to a result with units and reasoning; and laboratory observation to a chemical conclusion. This includes definitions, relationships, conditions, contrasts, particle and energy models, focused calculation steps, measurements, errors, and visible changes.

Selected reverse and contrast prompts appear only when the reverse direction has one clear standalone target. Mechanical permutations, graph-dependent prompts that need a missing figure, copied test formats, long multipart derivations, and visual recall tied to third-party figures are excluded. The review scheduler handles long-term spacing after installation.

The prompts, answers, examples, organization, metadata, and cover were created independently from common chemistry knowledge and original work. No protected questions, answer choices, scoring materials, curriculum prose, commercial card text, source figures, or third-party media were copied.

The Common knowledge · CC0 1.0 label applies only to the original prompts, answers, examples, organization, metadata, and cover, to the extent applicable rights exist. It does not claim ownership of scientific facts, equations, or third-party material.

Tarjetas de este mazo

  1. Tarjeta 1

    Pregunta

    What does one mole count?

    Respuesta

    Exactly 6.02214076 × 10^23 representative particles.

  2. Tarjeta 2

    Pregunta

    What does a peak in an element's mass spectrum represent?

    Respuesta

    An isotope with a particular mass-to-charge ratio; for singly charged monatomic ions, the position tracks isotopic mass.

  3. Tarjeta 3

    Pregunta

    What does an empirical formula show?

    Respuesta

    The lowest whole-number ratio of the elements' atoms in a compound.

  4. Tarjeta 4

    Pregunta

    How does a mixture differ from a pure substance at the particle level?

    Respuesta

    A mixture contains chemically distinct representative units in variable proportions; a pure substance contains one element or compound with fixed composition. Different isotopes do not make an elemental sample a mixture.

  5. Tarjeta 5

    Pregunta

    Which particles make up an atom's nucleus?

    Respuesta

    Protons and neutrons. Electrons occupy the space outside the nucleus.

  6. Tarjeta 6

    Pregunta

    What does a larger binding energy on a PES spectrum mean?

    Respuesta

    More energy is required to remove that electron, so it is held more strongly by the nucleus.

  7. Tarjeta 7

    Pregunta

    How does atomic radius generally change across a period and down a group?

    Respuesta

    It decreases from left to right as effective nuclear charge rises, and it increases down a group as additional electron shells increase distance and shielding.

  8. Tarjeta 8

    Pregunta

    What typical ion charge do Group 1 metals form?

    Respuesta

    +1, by losing their one valence electron.

  9. Tarjeta 9

    Pregunta

    How do you convert moles to particles?

    Respuesta

    Multiply by Avogadro's number: particles = moles × 6.022 × 10^23 mol^-1.

  10. Tarjeta 10

    Pregunta

    How is average atomic mass estimated from isotope data?

    Respuesta

    Add each isotopic mass multiplied by its fractional abundance.

  11. Tarjeta 11

    Pregunta

    How is an element's mass percent in a compound calculated?

    Respuesta

    Divide the mass contributed by that element by the compound's molar mass, then multiply by 100%.

  12. Tarjeta 12

    Pregunta

    How can measured elemental composition reveal a sample's purity?

    Respuesta

    Compare the measured mass fraction with the fraction expected for the pure compound; a mismatch indicates another component.

  13. Tarjeta 13

    Pregunta

    How do you build a ground-state electron configuration with the Aufbau principle?

    Respuesta

    For ordinary ground states, move through the periodic table in atomic-number order, filling each s, p, d, or f block as it appears. The subshell capacities are s², p⁶, d¹⁰, and f¹⁴. For example, Br is [Ar] 4s² 3d¹⁰ 4p⁵.

  14. Tarjeta 14

    Pregunta

    What does the relative area or height of an ideal PES peak indicate?

    Respuesta

    The relative number of electrons in the corresponding subshell.

  15. Tarjeta 15

    Pregunta

    How does first ionization energy generally change across a period and down a group?

    Respuesta

    It increases from left to right as effective nuclear charge rises, and it decreases down a group as distance and shielding make a valence electron easier to remove.

  16. Tarjeta 16

    Pregunta

    Why do elements in the same group form similar compounds?

    Respuesta

    Their ground-state valence patterns repeat, including which outer subshells are full or partly full. That leads to similar bonding and typical ion charges.

  17. Tarjeta 17

    Pregunta

    How do you convert a sample's mass to moles?

    Respuesta

    Divide its mass by its molar mass: n = m/M.

  18. Tarjeta 18

    Pregunta

    Which mass-spectrum interpretation lies outside the usual single-element model used in this deck?

    Respuesta

    Assigning peaks in mixtures or peaks from multiply charged or polyatomic species; the standard model uses singly charged monatomic ions of one element.

  19. Tarjeta 19

    Pregunta

    What does the law of definite proportions state?

    Respuesta

    Every pure sample of a given compound has the same element mass ratios.

  20. Tarjeta 20

    Pregunta

    Why can two samples of the same mixture have different compositions?

    Respuesta

    Mixture components are physically combined, so their relative amounts are not fixed by a chemical formula.

  21. Tarjeta 21

    Pregunta

    How does Coulomb's law connect charge and separation to attraction?

    Respuesta

    Attraction grows with the magnitude of the charge product and decreases with the square of the separation distance.

  22. Tarjeta 22

    Pregunta

    Which PES electrons usually appear at the highest binding energy?

    Respuesta

    Core electrons closest to the nucleus, because they feel the strongest nuclear attraction.

  23. Tarjeta 23

    Pregunta

    How does electron affinity generally change across a period and down a group?

    Respuesta

    Electron gain generally becomes more favorable from left to right across a period and less favorable down a group as distance and shielding increase. Stable subshell patterns create substantial exceptions.

  24. Tarjeta 24

    Pregunta

    Why are alkali metals generally more reactive down the group?

    Respuesta

    Their valence electron is farther from the nucleus and easier to remove.

  25. Tarjeta 25

    Pregunta

    How many moles are in 18.0 g of H₂O?

    Respuesta

    About 0.999 mol. Use 18.0 g ÷ 18.02 g mol^-1.

  26. Tarjeta 26

    Pregunta

    An element is 75% isotope 10 and 25% isotope 11; what is its average atomic mass?

    Respuesta

    10.25 u. Calculate (0.75 × 10) + (0.25 × 11).

  27. Tarjeta 27

    Pregunta

    A compound is 40.0% C, 6.7% H, and 53.3% O by mass; what is its empirical formula?

    Respuesta

    CH₂O. For a 100 g sample, convert each mass to moles and divide by the smallest amount.

  28. Tarjeta 28

    Pregunta

    A 10.0 g impure sample contains 8.5 g of the target compound; what is its mass-percent purity?

    Respuesta

    85%. Calculate (8.5 g ÷ 10.0 g) × 100%.

  29. Tarjeta 29

    Pregunta

    Which electrons are removed first when a transition metal forms a cation?

    Respuesta

    Electrons in the occupied orbital with the highest principal quantum number: 4s before 3d. For example, Fe²⁺ is [Ar] 3d⁶.

  30. Tarjeta 30

    Pregunta

    A PES spectrum has peaks proportional to 2, 2, and 6 electrons; which configuration fits?

    Respuesta

    1s² 2s² 2p⁶, the configuration of Ne.

  31. Tarjeta 31

    Pregunta

    How does electronegativity generally change across a period and down a group?

    Respuesta

    It increases from left to right across a period and decreases down a group as atomic size and shielding increase.

  32. Tarjeta 32

    Pregunta

    What empirical formula results from Al³⁺ and O²⁻?

    Respuesta

    Al₂O₃, because two Al³⁺ ions balance three O²⁻ ions.

  33. Tarjeta 33

    Pregunta

    How does a particle's mass in atomic mass units relate to its molar mass?

    Respuesta

    The numerical value is the same: a molecular or formula-unit mass of x u corresponds to a molar mass of x g mol^-1.

  34. Tarjeta 34

    Pregunta

    What does the tallest isotope peak usually indicate in a simple mass spectrum?

    Respuesta

    The most abundant isotope, assuming comparable detection response and singly charged ions.

  35. Tarjeta 35

    Pregunta

    How much oxygen is present in 25.0 g of a compound that is 32.0% oxygen by mass?

    Respuesta

    8.00 g O. Multiply 25.0 g by 0.320.

  36. Tarjeta 36

    Pregunta

    What does a particle diagram with two unbonded species in changing ratios represent?

    Respuesta

    A mixture, because more than one particle type is present and the ratio is not fixed in a formula unit.

  37. Tarjeta 37

    Pregunta

    What distinguishes valence electrons from core electrons?

    Respuesta

    Valence electrons are available for bonding or ion formation; main-group valence electrons occupy the outermost shell, while transition metals may also use (n−1)d electrons. Core electrons mainly shield nuclear charge.

  38. Tarjeta 38

    Pregunta

    Why can PES peak groups reveal an atom's occupied subshells?

    Respuesta

    Electrons in different subshells require distinct removal energies, producing separate binding-energy groups.

  39. Tarjeta 39

    Pregunta

    How do ion radii compare with neutral atoms and within an isoelectronic series?

    Respuesta

    Cations are smaller than their neutral atoms, while anions are larger. Among species with the same electron count, more protons pull the electrons closer and produce the smaller radius.

  40. Tarjeta 40

    Pregunta

    What formula is expected for a compound between a Group 2 metal M and a Group 17 nonmetal X?

    Respuesta

    MX₂, because M forms M²⁺ and X forms X⁻.

  41. Tarjeta 41

    Pregunta

    When is a covalent bond considered nonpolar?

    Respuesta

    When the bonded atoms have identical or very similar electronegativities, so the shared electron density is distributed approximately evenly.

  42. Tarjeta 42

    Pregunta

    Why does a bonded pair of atoms have an equilibrium bond length?

    Respuesta

    At that separation, attractive and repulsive interactions balance at minimum potential energy.

  43. Tarjeta 43

    Pregunta

    How are particles arranged in an ionic solid?

    Respuesta

    Cations and anions occupy a repeating three-dimensional lattice held by electrostatic attraction.

  44. Tarjeta 44

    Pregunta

    What model explains bonding in a metal?

    Respuesta

    Positive metal cores are held together by attraction to mobile, delocalized valence electrons.

  45. Tarjeta 45

    Pregunta

    How do you construct a Lewis diagram?

    Respuesta

    Count total valence electrons, adding electrons for a negative charge and subtracting them for a positive charge. Choose a skeleton, connect atoms with single bonds, complete terminal duets or octets, and place remaining electrons on the central atom. Add multiple bonds if needed, then check the electron total and formal charges.

  46. Tarjeta 46

    Pregunta

    What does resonance mean in a molecule or ion?

    Respuesta

    Resonance uses two or more valid Lewis diagrams with the same atom arrangement but different electron placement. The actual electron distribution is a hybrid; equivalent contributors have equal weight.

  47. Tarjeta 47

    Pregunta

    What determines molecular shape in VSEPR theory?

    Respuesta

    Electron domains around the central atom arrange to minimize repulsions.

  48. Tarjeta 48

    Pregunta

    How does an ionic bond differ from a covalent bond?

    Respuesta

    Ionic bonding is attraction among oppositely charged ions in an extended structure; covalent bonding uses shared electron density between atoms.

  49. Tarjeta 49

    Pregunta

    What happens to potential energy when bonded atoms are pushed much closer than equilibrium?

    Respuesta

    Potential energy rises sharply because nucleus–nucleus and electron–electron repulsions dominate.

  50. Tarjeta 50

    Pregunta

    Why are many ionic solids brittle?

    Respuesta

    A shifted lattice can align like charges, creating strong repulsion that splits the crystal.

  51. Tarjeta 51

    Pregunta

    What molecular shapes arise from two electron domains with no lone pairs and from three domains with zero or one lone pair?

    Respuesta

    Two bonding domains give linear with a 180° angle. Three domains with no lone pairs give trigonal planar with 120° angles; replacing one bond with a lone pair gives bent with an angle slightly below 120°.

  52. Tarjeta 52

    Pregunta

    Why are metals electrically conductive as solids?

    Respuesta

    Their delocalized electrons can move through the solid when an electric field is applied.

  53. Tarjeta 53

    Pregunta

    How is formal charge calculated for an atom in a Lewis diagram?

    Respuesta

    Formal charge = valence electrons − nonbonding electrons − half the bonding electrons.

  54. Tarjeta 54

    Pregunta

    Why can't electronegativity difference alone classify a bond as ionic or covalent?

    Respuesta

    Bonding lies on a continuum. A larger difference means more ionic character, but the element types and especially the compound's properties give the best classification.

  55. Tarjeta 55

    Pregunta

    Which shapes and bond-angle trends arise as lone pairs replace bonds in four electron domains?

    Respuesta

    Four bonds give tetrahedral with ideal 109.5° angles. One lone pair gives trigonal pyramidal with smaller angles; two lone pairs give bent with typically smaller angles again because lone pairs repel more strongly than bonding pairs.

  56. Tarjeta 56

    Pregunta

    What feature of a potential-energy curve represents bond dissociation energy?

    Respuesta

    The energy difference from the curve's minimum to the separated-atoms limit.

  57. Tarjeta 57

    Pregunta

    When does an ionic compound conduct electricity?

    Respuesta

    When molten or dissolved so its ions can move; not as a rigid solid lattice.

  58. Tarjeta 58

    Pregunta

    What is a substitutional alloy?

    Respuesta

    An alloy in which atoms of a similar size replace some host-metal atoms in the lattice.

  59. Tarjeta 59

    Pregunta

    How do two, three, and four electron domains map to hybridization?

    Respuesta

    Two domains map to sp, three to sp², and four to sp³, with ideal angles of 180°, 120°, and 109.5°. Hybridization involving d orbitals is outside this deck’s scope.

  60. Tarjeta 60

    Pregunta

    What usually makes one resonance contributor more favorable than another?

    Respuesta

    Smaller formal-charge magnitudes, appropriate negative charge on more electronegative atoms, and complete valence shells where applicable.

  61. Tarjeta 61

    Pregunta

    How many sigma and pi bonds are in single, double, and triple bonds?

    Respuesta

    A single bond has one sigma bond; a double has one sigma and one pi bond; a triple has one sigma and two pi bonds. Head-on sigma overlap is stronger than side-by-side pi overlap.

  62. Tarjeta 62

    Pregunta

    Why is a polar covalent bond polar?

    Respuesta

    Unequal electronegativity creates an uneven sharing of electron density and partial charges.

  63. Tarjeta 63

    Pregunta

    Which molecular shapes arise as lone pairs replace bonds in five electron domains?

    Respuesta

    Five bonds give trigonal bipyramidal; four bonds and one lone pair give seesaw; three bonds and two lone pairs give T-shaped; two bonds and three lone pairs give linear.

  64. Tarjeta 64

    Pregunta

    How do ionic charge and ionic radius affect attraction between ions?

    Respuesta

    Larger charge magnitudes and smaller ionic radii produce stronger attraction because the charge product increases and the ion centers are closer.

  65. Tarjeta 65

    Pregunta

    Why do ionic solids often have high melting points?

    Respuesta

    Many strong Coulombic attractions throughout the lattice must be overcome to free the ions.

  66. Tarjeta 66

    Pregunta

    What is an interstitial alloy?

    Respuesta

    A smaller atom occupies holes between host-metal atoms, often making lattice layers harder to slide.

  67. Tarjeta 67

    Pregunta

    What shape has six bonding domains and no lone pairs on the central atom?

    Respuesta

    Octahedral.

  68. Tarjeta 68

    Pregunta

    Which elements commonly form incomplete octets in stable Lewis diagrams?

    Respuesta

    Hydrogen forms a duet, and electron-deficient central atoms such as boron or beryllium can have fewer than eight electrons.

  69. Tarjeta 69

    Pregunta

    How do bond order and atomic size affect covalent bond length and strength?

    Respuesta

    Within a comparable bond family, higher bond order gives shorter, stronger bonds. Larger bonded atoms generally give longer bonds, which are often weaker because their orbitals overlap less effectively.

  70. Tarjeta 70

    Pregunta

    What bonding model best fits a sample that is malleable and conducts as a solid?

    Respuesta

    Metallic bonding with mobile, delocalized electrons and nondirectional attractions.

  71. Tarjeta 71

    Pregunta

    What shape has six electron domains, five bonds, and one lone pair?

    Respuesta

    Square pyramidal.

  72. Tarjeta 72

    Pregunta

    Which lattice should have stronger attractions: MgO or NaCl, assuming similar separations?

    Respuesta

    MgO, because the charge product for Mg²⁺ and O²⁻ is larger than for Na⁺ and Cl⁻.

  73. Tarjeta 73

    Pregunta

    Why are pure metals often malleable?

    Respuesta

    Metal cores can shift while the mobile electron sea maintains nondirectional attraction instead of exposing fixed like-charge planes.

  74. Tarjeta 74

    Pregunta

    What is the best Lewis structure for CO₂?

    Respuesta

    O=C=O, with two lone pairs on each oxygen and no formal charges.

  75. Tarjeta 75

    Pregunta

    What shape has six electron domains, four bonds, and two opposite lone pairs?

    Respuesta

    Square planar.

  76. Tarjeta 76

    Pregunta

    What limitation does an odd total number of valence electrons create for a Lewis diagram?

    Respuesta

    At least one electron must remain unpaired, so not every atom can have a complete paired-electron octet.

  77. Tarjeta 77

    Pregunta

    What does a higher bond order do to a bond's potential-energy curve?

    Respuesta

    It generally places the minimum at a shorter internuclear distance and makes the well deeper, corresponding to a shorter bond and a larger bond-dissociation energy.

  78. Tarjeta 78

    Pregunta

    When can a carbon–carbon double bond produce geometric isomers?

    Respuesta

    When each carbon has two different substituents. The pi bond restricts rotation, so distinct spatial arrangements can persist.

  79. Tarjeta 79

    Pregunta

    When may a third-period central atom exceed an octet in a Lewis diagram?

    Respuesta

    When the valid electron count and lower formal charges favor an expanded valence shell, as in species such as SF₆.

  80. Tarjeta 80

    Pregunta

    How do you decide whether a molecule with polar bonds is polar overall?

    Respuesta

    Add the bond-dipole vectors using the molecular shape; symmetry may cancel them, while an asymmetric arrangement leaves a net dipole.

  81. Tarjeta 81

    Pregunta

    Which interparticle forces act between all atoms and molecules?

    Respuesta

    London dispersion forces, caused by temporary and induced dipoles.

  82. Tarjeta 82

    Pregunta

    What four broad solid types does this deck compare?

    Respuesta

    Ionic, metallic, molecular, and covalent-network solids.

  83. Tarjeta 83

    Pregunta

    How do gas particles differ from liquid particles?

    Respuesta

    Gas particles are much farther apart and move independently; liquid particles stay close but can move past one another.

  84. Tarjeta 84

    Pregunta

    What relationship connects pressure, volume, amount, and temperature for an ideal gas?

    Respuesta

    PV = nRT, with absolute temperature in kelvins and units consistent with R.

  85. Tarjeta 85

    Pregunta

    What does temperature measure in kinetic molecular theory?

    Respuesta

    The particles' average translational kinetic energy.

  86. Tarjeta 86

    Pregunta

    What two ideal-gas assumptions fail most clearly for real gases?

    Respuesta

    Particles have nonzero volume and experience intermolecular attractions.

  87. Tarjeta 87

    Pregunta

    How is molarity defined?

    Respuesta

    Moles of solute per liter of solution: M = n/V.

  88. Tarjeta 88

    Pregunta

    What must a correct particulate diagram of NaCl(aq) show?

    Respuesta

    Separated Na⁺ and Cl⁻ ions in a 1:1 ratio, each surrounded by oriented water molecules.

  89. Tarjeta 89

    Pregunta

    Which separation method removes an insoluble solid from a liquid?

    Respuesta

    Filtration: the solid stays as residue while the liquid passes as filtrate.

  90. Tarjeta 90

    Pregunta

    What does “like dissolves like” mean at the particle level?

    Respuesta

    A solute tends to dissolve when new solute–solvent attractions can compete with the attractions disrupted in the pure substances.

  91. Tarjeta 91

    Pregunta

    What happens when matter absorbs electromagnetic radiation?

    Respuesta

    Its particles move to an allowed higher-energy state when the photon energy matches the energy gap.

  92. Tarjeta 92

    Pregunta

    Which equations connect photon energy, frequency, and wavelength?

    Respuesta

    E = hν and c = λν.

  93. Tarjeta 93

    Pregunta

    What is the Beer–Lambert law?

    Respuesta

    A = εbc: absorbance equals molar absorptivity at the chosen wavelength times path length times concentration.

  94. Tarjeta 94

    Pregunta

    What molecular features generally strengthen London dispersion forces?

    Respuesta

    More electrons and a more polarizable cloud strengthen temporary dipoles; greater contact area and accessible π-electron density can also strengthen the attraction.

  95. Tarjeta 95

    Pregunta

    Why do molecular solids usually have low melting points and fail to conduct electricity?

    Respuesta

    Distinct molecules are held together by relatively weak intermolecular forces, while their valence electrons stay localized in bonds and lone pairs.

  96. Tarjeta 96

    Pregunta

    How do particles move in a solid?

    Respuesta

    They vibrate about fixed positions and do not translate past one another.

  97. Tarjeta 97

    Pregunta

    What graph shapes connect V or P with T(K) or n for an ideal gas?

    Respuesta

    All four are straight lines through the origin: V versus T(K) at fixed n and P; P versus T(K) at fixed n and V; V versus n at fixed P and T; and P versus n at fixed V and T.

  98. Tarjeta 98

    Pregunta

    At the same temperature, which gas has the greater average molecular speed: He or Xe?

    Respuesta

    He. Both have the same average kinetic energy, but KE = ½mv² means the lower-mass particles move faster.

  99. Tarjeta 99

    Pregunta

    Why do real gases deviate more at high pressure?

    Respuesta

    Particles are crowded, so their own volume is no longer negligible compared with the container volume.

  100. Tarjeta 100

    Pregunta

    Which relationship describes dilution when solute amount is conserved?

    Respuesta

    M₁V₁ = M₂V₂.

  101. Tarjeta 101

    Pregunta

    Why does an aqueous ionic solution conduct electricity?

    Respuesta

    Dissolved ions are mobile and carry charge through the solution.

  102. Tarjeta 102

    Pregunta

    Which property lets simple distillation separate two liquids?

    Respuesta

    A sufficient difference in volatility or boiling point, so the vapor is enriched in the more volatile component.

  103. Tarjeta 103

    Pregunta

    Why are many ionic compounds soluble in water but poorly soluble in a nonpolar solvent?

    Respuesta

    Water can form strong ion–dipole attractions that stabilize separated ions; a nonpolar solvent cannot provide comparable attractions.

  104. Tarjeta 104

    Pregunta

    Which molecular transition is commonly associated with microwave absorption?

    Respuesta

    A transition between quantized rotational energy levels.

  105. Tarjeta 105

    Pregunta

    What frequency corresponds to a 600. nm photon?

    Respuesta

    5.00 × 10^14 s^-1. Use ν = c/λ with 600. nm = 6.00 × 10^-7 m.

  106. Tarjeta 106

    Pregunta

    What is the absorbance to two significant figures when ε = 2.0 × 10² L mol^-1 cm^-1, b = 1.00 cm, and c = 0.0020 M?

    Respuesta

    0.40. Use A = εbc.

  107. Tarjeta 107

    Pregunta

    What conditions allow hydrogen bonding between two molecules?

    Respuesta

    One molecule must donate an H covalently bonded to N, O, or F, and the other must provide a lone pair on N, O, or F. A molecule can be a donor, an acceptor, or both.

  108. Tarjeta 108

    Pregunta

    Why are covalent-network solids often very hard with high melting points?

    Respuesta

    A continuous network of strong covalent bonds must be disrupted to deform or melt the solid.

  109. Tarjeta 109

    Pregunta

    Why do a substance's solid and liquid phases usually have similar molar volumes?

    Respuesta

    Their particles remain in close contact in both phases, even though liquid particles can move past one another.

  110. Tarjeta 110

    Pregunta

    How is a gas mixture's total pressure related to its component pressures?

    Respuesta

    Ptotal = ΣPi; each partial pressure is the pressure that component would exert alone in the same volume and temperature.

  111. Tarjeta 111

    Pregunta

    What microscopic events create gas pressure?

    Respuesta

    Gas particles collide with container walls and transfer momentum.

  112. Tarjeta 112

    Pregunta

    Why do intermolecular attractions matter more for gases at low temperature?

    Respuesta

    Particles move more slowly, so attractions can alter their paths and promote condensation.

  113. Tarjeta 113

    Pregunta

    What is the final concentration after 50.0 mL of 2.00 M solution is diluted to 200.0 mL?

    Respuesta

    0.500 M. Use M₂ = M₁V₁/V₂.

  114. Tarjeta 114

    Pregunta

    What must a particulate representation of a solution communicate?

    Respuesta

    The relative concentrations of its components and the particle-level interactions among those components.

  115. Tarjeta 115

    Pregunta

    What causes components to separate in chromatography?

    Respuesta

    They differ in attraction to the stationary phase and the mobile phase, so they travel at different rates.

  116. Tarjeta 116

    Pregunta

    Why are many polar molecular solutes soluble in water?

    Respuesta

    Dipole attractions or hydrogen bonds with water can replace the solute–solute and water–water attractions disrupted during mixing.

  117. Tarjeta 117

    Pregunta

    Why does an atom produce discrete spectral lines?

    Respuesta

    Its electrons can occupy only quantized energy levels, so only photons matching allowed energy differences are absorbed or emitted.

  118. Tarjeta 118

    Pregunta

    How does photon energy change when frequency doubles?

    Respuesta

    It doubles because E = hν.

  119. Tarjeta 119

    Pregunta

    Why is a calibration curve useful in spectrophotometry?

    Respuesta

    It relates measured absorbance to known concentrations, letting an unknown concentration be read by interpolation within the linear range.

  120. Tarjeta 120

    Pregunta

    How does an ion–dipole attraction form, and how does it compare with dipole–dipole attraction?

    Respuesta

    An ion attracts the oppositely charged end of a polar molecule. Ion–dipole attractions tend to be stronger than dipole–dipole attractions.

  121. Tarjeta 121

    Pregunta

    Which solid type is usually both conductive and malleable?

    Respuesta

    A metallic solid, because its delocalized electrons move and its nondirectional bonding tolerates layer shifts.

  122. Tarjeta 122

    Pregunta

    How does a crystalline solid differ from an amorphous solid?

    Respuesta

    A crystalline solid has long-range repeating order; an amorphous solid lacks that long-range periodic arrangement.

  123. Tarjeta 123

    Pregunta

    How is a gas component's partial pressure found from mole fraction?

    Respuesta

    Pi = XiPtotal.

  124. Tarjeta 124

    Pregunta

    How does heating a fixed-volume gas affect its pressure in the ideal model?

    Respuesta

    Pressure rises because faster particles collide with the walls more forcefully and frequently.

  125. Tarjeta 125

    Pregunta

    Why can attractions make a real gas's measured pressure lower than the ideal prediction?

    Respuesta

    Attractions pull approaching particles away from the walls, reducing momentum transfer during wall collisions.

  126. Tarjeta 126

    Pregunta

    How many moles of ions result from complete dissolution of 0.20 mol CaCl₂?

    Respuesta

    0.60 mol ions: 0.20 mol Ca²⁺ plus 0.40 mol Cl⁻.

  127. Tarjeta 127

    Pregunta

    How should water orient around Cl⁻ in a particle model?

    Respuesta

    Its partially positive hydrogen ends point toward Cl⁻.

  128. Tarjeta 128

    Pregunta

    Can filtration separate dissolved components of a liquid solution?

    Respuesta

    No. Dissolved particles pass through the filter with the solvent; filtration only retains an insoluble solid.

  129. Tarjeta 129

    Pregunta

    Why do nonpolar molecular solutes often dissolve in nonpolar solvents?

    Respuesta

    Both rely mainly on compatible London dispersion forces, so mixing can replace the attractions disrupted in the separate substances.

  130. Tarjeta 130

    Pregunta

    What does a shorter absorbed wavelength imply about an energy transition?

    Respuesta

    A larger energy gap because E = hc/λ.

  131. Tarjeta 131

    Pregunta

    What is the energy of a photon with frequency 5.0 × 10^14 s^-1?

    Respuesta

    3.3 × 10^-19 J. Multiply by Planck's constant: E = (6.626 × 10^-34 J·s)(5.0 × 10^14 s^-1).

  132. Tarjeta 132

    Pregunta

    How does doubling cuvette path length affect absorbance in the linear Beer–Lambert range?

    Respuesta

    Absorbance doubles if concentration and molar absorptivity stay constant.

  133. Tarjeta 133

    Pregunta

    How can noncovalent interactions affect a large biomolecule?

    Respuesta

    Attractions between molecules or between different regions of the same molecule help set its shape, which strongly affects its properties and function.

  134. Tarjeta 134

    Pregunta

    Why does an ionic solid usually fail to conduct as a solid?

    Respuesta

    Its ions are fixed in lattice positions. The same substance conducts when molten or dissolved because the ions can then move.

  135. Tarjeta 135

    Pregunta

    Why does a gas have no definite shape or volume?

    Respuesta

    Its widely spaced particles move constantly and experience minimal interparticle attraction, so they spread through the available container.

  136. Tarjeta 136

    Pregunta

    What graph shapes show the inverse pressure–volume relationship for a fixed amount of ideal gas at constant temperature?

    Respuesta

    A plot of P against V is a decreasing curve, while P against 1/V is a straight line through the origin.

  137. Tarjeta 137

    Pregunta

    At the same temperature, do different ideal gases have different average kinetic energies?

    Respuesta

    No. Average translational kinetic energy depends only on absolute temperature.

  138. Tarjeta 138

    Pregunta

    Under which conditions is ideal-gas behavior most accurate?

    Respuesta

    Low pressure and high temperature, where particles are far apart and attractions matter least.

  139. Tarjeta 139

    Pregunta

    What particle-level feature distinguishes a solution from a heterogeneous mixture?

    Respuesta

    A solution—whether solid, liquid, or gas—is uniform throughout; a heterogeneous mixture has regions or phases with different compositions.

  140. Tarjeta 140

    Pregunta

    How should water orient around Na⁺ in a particulate model?

    Respuesta

    Its partially negative oxygen end points toward Na⁺.

  141. Tarjeta 141

    Pregunta

    In paper chromatography, why does one solute spot travel farther than another?

    Respuesta

    It interacts more strongly with the mobile phase or more weakly with the stationary phase. With known phase polarities, that travel difference can reveal relative solute polarity.

  142. Tarjeta 142

    Pregunta

    What energy competition helps explain whether an ionic solid dissolves?

    Respuesta

    The energy needed to separate lattice ions competes with the energy released when ion–solvent attractions form.

  143. Tarjeta 143

    Pregunta

    Which molecular motions commonly absorb infrared radiation?

    Respuesta

    Bond vibrations whose changing dipole can interact with the radiation.

  144. Tarjeta 144

    Pregunta

    Why must wavelength be converted to meters in c = λν when c is in m s^-1?

    Respuesta

    Consistent units are required so meters cancel correctly and frequency comes out in s^-1.

  145. Tarjeta 145

    Pregunta

    How can fingerprints on a cuvette affect a visible-light absorbance reading?

    Respuesta

    They can absorb or scatter extra light, making measured absorbance too high and the inferred concentration too high.

  146. Tarjeta 146

    Pregunta

    What causes and controls the strength of dipole–dipole attractions?

    Respuesta

    Opposite partial charges on neighboring polar molecules attract. Strength increases with larger molecular dipoles and depends on how favorably the dipoles are oriented.

  147. Tarjeta 147

    Pregunta

    Why is graphite conductive and soft while diamond is insulating and hard?

    Respuesta

    Graphite has delocalized electrons within its sheets, so it conducts, and its layers can slide, so it is soft. Diamond has a rigid three-dimensional network of localized covalent bonds, making it hard and insulating.

  148. Tarjeta 148

    Pregunta

    Why are gases much more compressible than liquids?

    Respuesta

    Gas particles have large empty spaces between them; liquid particles are already close together.

  149. Tarjeta 149

    Pregunta

    What volume does 0.500 mol CO₂ occupy at 1.00 atm and 300. K if it behaves ideally?

    Respuesta

    12.3 L. Use V = nRT/P = (0.500 mol)(0.08206 L atm mol^-1 K^-1)(300. K)/(1.00 atm).

  150. Tarjeta 150

    Pregunta

    Why does a lighter gas effuse faster than a heavier gas at the same temperature?

    Respuesta

    Its particles have a higher average speed because equal average kinetic energy is shared by less mass.

  151. Tarjeta 151

    Pregunta

    How does finite particle volume affect a real gas at very high pressure?

    Respuesta

    The free volume available for particle motion is smaller than the container volume assumed by the ideal model.

  152. Tarjeta 152

    Pregunta

    How should 250.0 mL of 0.100 M NaCl be prepared from solid NaCl?

    Respuesta

    Dissolve 0.0250 mol NaCl, or 1.46 g, then dilute to exactly 250.0 mL in a volumetric flask.

  153. Tarjeta 153

    Pregunta

    What changes in a particle diagram when a solution is diluted without losing solute?

    Respuesta

    The solute-particle count stays constant while solvent volume and particle spacing increase.

  154. Tarjeta 154

    Pregunta

    Why is fractional distillation better than simple distillation for liquids with close boiling points?

    Respuesta

    Repeated vaporization–condensation steps enrich the vapor in the more volatile component more effectively.

  155. Tarjeta 155

    Pregunta

    Why are oil and water usually immiscible?

    Respuesta

    Water's strong hydrogen-bond network isn't replaced by equally strong water–oil attractions, so the substances separate into phases.

  156. Tarjeta 156

    Pregunta

    Which molecular transition is commonly associated with ultraviolet or visible absorption?

    Respuesta

    A transition between electronic energy levels.

  157. Tarjeta 157

    Pregunta

    Which photon carries more energy, blue light or red light?

    Respuesta

    Blue light, because it has shorter wavelength and higher frequency.

  158. Tarjeta 158

    Pregunta

    Why is absorbance often measured at the wavelength of maximum absorbance in Beer–Lambert analysis?

    Respuesta

    It gives the largest concentration-sensitive signal, and the flat top near the maximum makes small wavelength-setting errors less influential.

  159. Tarjeta 159

    Pregunta

    What creates a dipole–induced-dipole attraction, and what controls its strength?

    Respuesta

    A permanent dipole distorts a nearby nonpolar particle's electron cloud and creates an attractive temporary dipole. A larger permanent dipole and a more polarizable nonpolar partner make the attraction stronger.

  160. Tarjeta 160

    Pregunta

    How do stronger intermolecular forces affect vapor pressure, boiling point, and melting point?

    Respuesta

    They lower vapor pressure and raise boiling point. Melting point often rises too, but the trend is less direct because melting rearranges rather than fully separates particles.

  161. Tarjeta 161

    Pregunta

    How do particles behave in a liquid?

    Respuesta

    They stay in close contact while moving and colliding continuously. Temperature and interparticle attractions affect their arrangement and motion.

  162. Tarjeta 162

    Pregunta

    Why must Celsius temperature be converted to kelvins in gas-law calculations?

    Respuesta

    Gas-law proportionalities require an absolute temperature scale whose zero corresponds to zero extrapolated thermal motion.

  163. Tarjeta 163

    Pregunta

    How does raising temperature change a Maxwell–Boltzmann speed distribution?

    Respuesta

    The distribution broadens, its peak lowers and shifts right, and a larger fraction of particles have high speed.

  164. Tarjeta 164

    Pregunta

    Why does the ideal-gas model treat collisions as elastic?

    Respuesta

    It assumes total kinetic energy is conserved in particle–particle and particle–wall collisions.

  165. Tarjeta 165

    Pregunta

    How many moles of solute are in 75.0 mL of a 0.400 M solution?

    Respuesta

    0.0300 mol. Multiply 0.400 mol L^-1 by 0.0750 L.

  166. Tarjeta 166

    Pregunta

    For equal solution volumes drawn at the same scale, what shows which solution is more concentrated?

    Respuesta

    The more concentrated diagram contains more solute particles in that equal volume.

  167. Tarjeta 167

    Pregunta

    How do differences in intermolecular attractions let distillation separate a liquid solution?

    Respuesta

    They give the components different vapor pressures, so the vapor is enriched in the more volatile component.

  168. Tarjeta 168

    Pregunta

    What comparison helps predict whether two liquids will be miscible?

    Respuesta

    Liquids with similar types and strengths of intermolecular attractions are more likely to mix uniformly.

  169. Tarjeta 169

    Pregunta

    How can an absorption spectrum help identify a substance?

    Respuesta

    Its allowed energy gaps produce a characteristic pattern of absorbed wavelengths that can be compared with known spectra.

  170. Tarjeta 170

    Pregunta

    How does absorbing or emitting a photon change an atom's or molecule's energy?

    Respuesta

    Absorption raises the species' energy by exactly the photon energy; emission lowers it by the same amount.

  171. Tarjeta 171

    Pregunta

    What macroscopic evidence can support that a chemical reaction occurred?

    Respuesta

    Evidence can include gas formation, precipitate formation, a persistent color change, or an energy change, interpreted with particle-level changes.

  172. Tarjeta 172

    Pregunta

    What does a net ionic equation include?

    Respuesta

    Only the dissolved or reacting species that undergo chemical change; spectator ions are omitted.

  173. Tarjeta 173

    Pregunta

    What must a correct particulate reaction diagram conserve?

    Respuesta

    The number of atoms of every element and the total charge.

  174. Tarjeta 174

    Pregunta

    What distinguishes a chemical change from a physical change?

    Respuesta

    A chemical change rearranges bonds into new substances; a physical change alters state or arrangement without changing chemical identity.

  175. Tarjeta 175

    Pregunta

    What does a balanced equation's coefficient ratio provide?

    Respuesta

    The mole ratio among reacting and produced species.

  176. Tarjeta 176

    Pregunta

    What is the equivalence point of a titration?

    Respuesta

    The point where titrant and analyte have reacted in the stoichiometric ratio given by the balanced equation.

  177. Tarjeta 177

    Pregunta

    What defines a precipitation reaction?

    Respuesta

    Aqueous ions combine to form a sparingly soluble solid.

  178. Tarjeta 178

    Pregunta

    What happens in a Brønsted–Lowry acid–base reaction?

    Respuesta

    A proton transfers from the acid (donor) to the base (acceptor). In aqueous solution, H₂O can play either role.

  179. Tarjeta 179

    Pregunta

    What does oxidation mean in a redox reaction?

    Respuesta

    Loss of electrons and an increase in oxidation number.

  180. Tarjeta 180

    Pregunta

    What particle-level change confirms that a process is chemical?

    Respuesta

    Atoms rearrange into new combinations, producing substances with different compositions.

  181. Tarjeta 181

    Pregunta

    Which ions are spectators when AgNO₃(aq) reacts with NaCl(aq)?

    Respuesta

    Na⁺ and NO₃⁻. The net ionic reaction is Ag⁺(aq) + Cl⁻(aq) → AgCl(s).

  182. Tarjeta 182

    Pregunta

    How does a particulate diagram reveal the limiting reactant?

    Respuesta

    After forming the maximum product allowed by the ratio, none of the limiting reactant remains while excess reactant particles do.

  183. Tarjeta 183

    Pregunta

    Is melting ice a chemical or physical change?

    Respuesta

    A physical change. H₂O molecules remain H₂O while their arrangement and motion change.

  184. Tarjeta 184

    Pregunta

    How is the limiting reactant identified from given amounts?

    Respuesta

    Convert each reactant to the same product amount using the balanced equation; the smaller product amount identifies the limiting reactant.

  185. Tarjeta 185

    Pregunta

    How does an endpoint differ from an equivalence point?

    Respuesta

    The endpoint is an observed signal such as indicator color change; the equivalence point is the exact stoichiometric condition.

  186. Tarjeta 186

    Pregunta

    How is complete combustion of a hydrocarbon in excess oxygen classified, and what products form?

    Respuesta

    It is a redox combustion reaction that forms CO₂ and H₂O.

  187. Tarjeta 187

    Pregunta

    What are the conjugate acid and conjugate base in NH₃ + H₂O ⇌ NH₄⁺ + OH⁻?

    Respuesta

    NH₄⁺ is the conjugate acid of NH₃, and OH⁻ is the conjugate base of H₂O.

  188. Tarjeta 188

    Pregunta

    What does reduction mean in a redox reaction?

    Respuesta

    Gain of electrons and a decrease in oxidation number.

  189. Tarjeta 189

    Pregunta

    Which common changes are physical rather than chemical?

    Respuesta

    Phase changes and the formation or separation of mixtures are physical when each substance keeps its composition.

  190. Tarjeta 190

    Pregunta

    How are strong soluble electrolytes written in a complete ionic equation?

    Respuesta

    As separated aqueous ions; solids, liquids, gases, and weak electrolytes stay intact.

  191. Tarjeta 191

    Pregunta

    A diagram starts with six A particles and four B₂ particles for 2A + B₂ → 2AB; what remains after completion?

    Respuesta

    One B₂ remains. Six A consume three B₂ and form six AB.

  192. Tarjeta 192

    Pregunta

    Why is dissolving NaCl in water normally classified as a physical change?

    Respuesta

    Na⁺ and Cl⁻ separate and become hydrated, but retain their chemical identities. Removing the water recovers NaCl; the shift from ion–ion to ion–dipole attractions does not by itself form a new substance.

  193. Tarjeta 193

    Pregunta

    What mass of AgCl can form from 25.0 mL of 0.200 M AgNO₃ mixed with excess Cl⁻?

    Respuesta

    0.717 g AgCl. The 1:1 reaction gives 0.00500 mol AgCl; multiply by 143.32 g mol^-1.

  194. Tarjeta 194

    Pregunta

    What calculation finds unknown analyte moles at equivalence?

    Respuesta

    Use titrant moles, n = MV, then apply the balanced-reaction mole ratio.

  195. Tarjeta 195

    Pregunta

    Which feature identifies an acid–base, redox, or precipitation reaction?

    Respuesta

    Acid–base reactions transfer protons, redox reactions change oxidation numbers through electron transfer, and precipitation reactions form a sparingly soluble solid.

  196. Tarjeta 196

    Pregunta

    What is the net ionic equation for strong acid–strong base neutralization?

    Respuesta

    H⁺(aq) + OH⁻(aq) → H₂O(l).

  197. Tarjeta 197

    Pregunta

    What is the oxidation number of sulfur in SO₄²⁻?

    Respuesta

    +6. Four oxygens contribute -8 total, so sulfur must be +6 to give -2 overall.

  198. Tarjeta 198

    Pregunta

    Why can gas bubbles alone be ambiguous evidence of reaction?

    Respuesta

    Bubbles may also come from boiling or dissolved gas escaping, so the context and particle identities must support a chemical change.

  199. Tarjeta 199

    Pregunta

    How is melting ice represented as a balanced physical-change equation?

    Respuesta

    H₂O(s) → H₂O(l). The formula and atom count stay the same because only the physical state changes.

  200. Tarjeta 200

    Pregunta

    What does a particle diagram show when no reaction occurs after two aqueous ionic solutions mix?

    Respuesta

    All ions remain separated and solvated, with no new bonded particles, precipitate, or gas.

  201. Tarjeta 201

    Pregunta

    Why is rusting iron a chemical change?

    Respuesta

    Iron atoms form new iron-oxide substances through electron transfer and new bonding.

  202. Tarjeta 202

    Pregunta

    For 2H₂O₂(aq) → 2H₂O(l) + O₂(g), what volume of O₂ forms from 0.100 mol H₂O₂ at 298 K and 1.00 atm?

    Respuesta

    1.22 L O₂. The mole ratio gives 0.0500 mol O₂, then V = nRT/P.

  203. Tarjeta 203

    Pregunta

    A 25.0 mL monoprotic acid sample requires 20.0 mL of 0.150 M NaOH; what is the acid concentration?

    Respuesta

    0.120 M. At 1:1 equivalence, moles acid = 0.0200 L × 0.150 M, then divide by 0.0250 L.

  204. Tarjeta 204

    Pregunta

    Which salts does the minimum solubility rule in this deck treat as soluble?

    Respuesta

    All salts containing Na⁺, K⁺, NH₄⁺, or NO₃⁻ are treated as soluble in water.

  205. Tarjeta 205

    Pregunta

    How are the strengths of a conjugate acid and its conjugate base related?

    Respuesta

    A stronger acid has a weaker conjugate base, and a stronger base has a weaker conjugate acid.

  206. Tarjeta 206

    Pregunta

    How are oxidation and reduction half-reactions combined into one balanced equation?

    Respuesta

    Multiply them so electrons lost equal electrons gained, add the half-reactions, then cancel electrons and any identical species on both sides.

  207. Tarjeta 207

    Pregunta

    How do molecular, complete ionic, and net ionic equations differ?

    Respuesta

    Molecular equations keep compounds intact, complete ionic equations split strong soluble electrolytes, and net ionic equations remove spectators. All three conserve atoms and charge.

  208. Tarjeta 208

    Pregunta

    How should coefficients change particle counts in a reaction diagram?

    Respuesta

    They set whole-particle ratios while preserving each particle's chemical formula.

  209. Tarjeta 209

    Pregunta

    Is separating a mixture by distillation a chemical or physical change?

    Respuesta

    A physical change. Components change phase and location but keep their chemical identities.

  210. Tarjeta 210

    Pregunta

    What equation results from Cu → Cu²⁺ + 2e⁻ and Ag⁺ + e⁻ → Ag?

    Respuesta

    Cu + 2Ag⁺ → Cu²⁺ + 2Ag. Multiply the silver half-reaction by 2 and cancel 2e⁻; both atom counts and net charge then match.

  211. Tarjeta 211

    Pregunta

    How is average reaction rate found from a reactant concentration?

    Respuesta

    Use the negative concentration change divided by elapsed time, adjusted by its stoichiometric coefficient when comparing species rates.

  212. Tarjeta 212

    Pregunta

    What does a rate law express?

    Respuesta

    It shows how the measured rate depends on reactant concentrations. In rate = k[A]^m[B]^n, m and n are the orders in A and B, and m + n is the overall order.

  213. Tarjeta 213

    Pregunta

    A plot of ln[A] versus time is linear; what is the order in A and its integrated rate law?

    Respuesta

    First order: ln[A]t = ln[A]0 − kt, so the plot's slope is −k.

  214. Tarjeta 214

    Pregunta

    What is an elementary reaction?

    Respuesta

    A single step in a mechanism whose rate law follows directly from its reactant molecularity.

  215. Tarjeta 215

    Pregunta

    What two collision conditions are needed for reaction?

    Respuesta

    Sufficient collision energy and a productive molecular orientation.

  216. Tarjeta 216

    Pregunta

    What does activation energy represent on a reaction-energy profile?

    Respuesta

    The energy difference from the reactants to the transition state. The reaction coordinate tracks the step's structural progress, not elapsed time.

  217. Tarjeta 217

    Pregunta

    What must the elementary steps of a valid mechanism do when added?

    Respuesta

    Cancel intermediates and reproduce the overall balanced reaction.

  218. Tarjeta 218

    Pregunta

    How is a proposed mechanism tested against kinetics?

    Respuesta

    Its derived rate law must agree with the experimentally measured rate law.

  219. Tarjeta 219

    Pregunta

    What does a pre-equilibrium approximation assume?

    Respuesta

    A fast reversible step reaches equilibrium before a later slow step consumes its intermediate.

  220. Tarjeta 220

    Pregunta

    What does each peak on a multistep energy profile represent?

    Respuesta

    A transition state for one elementary step.

  221. Tarjeta 221

    Pregunta

    How does a catalyst increase reaction rate?

    Respuesta

    It provides an alternate mechanism with a lower activation-energy pathway.

  222. Tarjeta 222

    Pregunta

    Why does crushing a solid reactant usually increase its reaction rate?

    Respuesta

    Crushing increases exposed surface area, so more reactant particles can collide with the other reactant each second.

  223. Tarjeta 223

    Pregunta

    How is reaction order found from initial-rate data?

    Respuesta

    Compare trials where one reactant concentration changes while the others stay constant, then match the rate factor to the concentration factor.

  224. Tarjeta 224

    Pregunta

    A plot of [A] versus time is linear; what is the order in A and its integrated rate law?

    Respuesta

    Zero order: [A]t = [A]0 − kt, so the plot's slope is −k.

  225. Tarjeta 225

    Pregunta

    What is the rate law for the elementary step 2A + B → products?

    Respuesta

    rate = k[A]²[B]. This inference is valid because the step is elementary.

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  226. Tarjeta 226

    Pregunta

    How does raising temperature change a Maxwell–Boltzmann energy distribution and reaction rate?

    Respuesta

    The distribution shifts and broadens toward higher energies, so a larger fraction of collisions exceeds the activation-energy threshold and can react.

  227. Tarjeta 227

    Pregunta

    How is ΔH read from a reaction-energy profile?

    Respuesta

    ΔH = energy of products − energy of reactants.

  228. Tarjeta 228

    Pregunta

    What is a reaction intermediate?

    Respuesta

    A species formed in one mechanism step and consumed in a later step, so it cancels from the overall equation.

  229. Tarjeta 229

    Pregunta

    Why can't overall reaction coefficients usually supply rate-law exponents?

    Respuesta

    The overall equation hides the mechanism; exponents come from experiment unless the reaction is a stated elementary step.

  230. Tarjeta 230

    Pregunta

    How does pre-equilibrium remove an intermediate from a rate law?

    Respuesta

    Use the fast-step equilibrium relation to express the intermediate concentration in terms of stable reactants.

  231. Tarjeta 231

    Pregunta

    What does each valley between peaks represent on a multistep profile?

    Respuesta

    A reaction intermediate.

  232. Tarjeta 232

    Pregunta

    Does a catalyst change ΔH or the equilibrium constant?

    Respuesta

    No. It changes the pathway and rates, not reactant/product energies or the equilibrium composition.

  233. Tarjeta 233

    Pregunta

    For 2A → B, how are disappearance of A and appearance of B related?

    Respuesta

    Reaction rate = -(1/2)Δ[A]/Δt = Δ[B]/Δt.

  234. Tarjeta 234

    Pregunta

    How do the units of k depend on a rate law's overall order?

    Respuesta

    They must make the rate unit M s^-1: zero order uses M s^-1, first order s^-1, and second order M^-1 s^-1.

  235. Tarjeta 235

    Pregunta

    A plot of 1/[A] versus time is linear; what is the order in A and its integrated rate law?

    Respuesta

    Second order: 1/[A]t = 1/[A]0 + kt, so the plot's slope is +k.

  236. Tarjeta 236

    Pregunta

    What is molecularity?

    Respuesta

    The number of reacting particles in an elementary step, such as unimolecular or bimolecular.

  237. Tarjeta 237

    Pregunta

    How does raising temperature affect k in the qualitative Arrhenius model?

    Respuesta

    k increases, often sharply, because a larger fraction of collisions can reach the transition state. Arrhenius-equation calculations are outside this deck’s scope.

  238. Tarjeta 238

    Pregunta

    A reactant falls from 0.80 M to 0.50 M in 30. s; what is its average disappearance rate to two significant figures?

    Respuesta

    0.010 M s^-1. Use -(0.50 − 0.80) M ÷ 30. s.

  239. Tarjeta 239

    Pregunta

    How does a catalyst differ from an intermediate in a mechanism?

    Respuesta

    A catalyst is consumed early and regenerated later; an intermediate is formed early and consumed later.

  240. Tarjeta 240

    Pregunta

    For 2NO₂ → NO₃ + NO (slow), followed by NO₃ + CO → NO₂ + CO₂ (fast), what rate law is predicted?

    Respuesta

    rate = k[NO₂]². The first step is elementary and rate-limiting, so its molecularity sets the observed rate law.

  241. Tarjeta 241

    Pregunta

    On a multistep reaction-energy profile, which feature often identifies the rate-determining step?

    Respuesta

    The step with the largest activation barrier measured from its preceding valley to its peak.

  242. Tarjeta 242

    Pregunta

    If changing [B] leaves rate unchanged, what is the order in B?

    Respuesta

    Zero order, so [B]^0 = 1 in the measured rate law.

  243. Tarjeta 243

    Pregunta

    What mechanism changes can binding, acid–base, or surface catalysis introduce?

    Respuesta

    They can orient reactants, lower activation barriers, or create new bound, protonated, or deprotonated intermediates and elementary steps; the catalyst is regenerated.

  244. Tarjeta 244

    Pregunta

    What is special about a first-order reaction's half-life?

    Respuesta

    It is constant and independent of starting concentration: t1/2 = ln 2/k. Radioactive decay is a common first-order example.

  245. Tarjeta 245

    Pregunta

    Why is a termolecular elementary collision uncommon?

    Respuesta

    Three particles must collide simultaneously with suitable energy and orientation, which is much less probable than one- or two-particle events.

  246. Tarjeta 246

    Pregunta

    On a reaction-energy profile, how are reverse activation energy, forward activation energy, and ΔH related?

    Respuesta

    Ea,reverse = Ea,forward − ΔH. The reverse barrier is measured from products to the same transition state.

  247. Tarjeta 247

    Pregunta

    Why can correct orientation matter even above the activation energy?

    Respuesta

    The colliding reactive sites must align so old bonds can break and new bonds can form along the reaction pathway.

  248. Tarjeta 248

    Pregunta

    How does detecting a proposed reaction intermediate affect a mechanism claim?

    Respuesta

    It supports a mechanism that contains that intermediate, but it doesn't prove that mechanism is unique.

  249. Tarjeta 249

    Pregunta

    For 2NO ⇌ N₂O₂ (fast equilibrium), followed by N₂O₂ + O₂ → 2NO₂ (slow), what observed rate law results?

    Respuesta

    rate = kobs[NO]²[O₂]. Start with rate = k₂[N₂O₂][O₂], use [N₂O₂] = K[NO]² from the fast equilibrium, then substitute.

  250. Tarjeta 250

    Pregunta

    What does the highest point of a one-step energy profile represent?

    Respuesta

    The transition state, an unstable arrangement at the top of the activation barrier.

  251. Tarjeta 251

    Pregunta

    What sign does q have for an endothermic system?

    Respuesta

    Positive, because the system absorbs heat from the surroundings.

  252. Tarjeta 252

    Pregunta

    How does an exothermic reaction appear on an enthalpy diagram?

    Respuesta

    Products lie below reactants, so ΔH is negative.

  253. Tarjeta 253

    Pregunta

    What condition defines thermal equilibrium?

    Respuesta

    Objects in contact have the same temperature, so there is no net heat transfer.

  254. Tarjeta 254

    Pregunta

    What equations relate heat capacity and temperature change to heat transfer?

    Respuesta

    Use q = mcΔT with specific heat capacity, or q = nCₘΔT with molar heat capacity.

  255. Tarjeta 255

    Pregunta

    Why is temperature constant during a phase-change plateau?

    Respuesta

    Added or removed energy changes interparticle potential energy instead of average kinetic energy.

  256. Tarjeta 256

    Pregunta

    What does ΔHrxn describe?

    Respuesta

    The heat absorbed or released at constant pressure for the reaction exactly as written under the stated conditions.

  257. Tarjeta 257

    Pregunta

    How is reaction enthalpy estimated from average bond enthalpies?

    Respuesta

    ΔHrxn ≈ Σ(bonds broken) − Σ(bonds formed).

  258. Tarjeta 258

    Pregunta

    What is the standard enthalpy of formation of an element in its standard state?

    Respuesta

    Zero by definition.

  259. Tarjeta 259

    Pregunta

    In a Hess’s law calculation, how should a step change when the target needs twice its reverse?

    Respuesta

    Reverse the equation, double every coefficient, and multiply its ΔH by -2.

  260. Tarjeta 260

    Pregunta

    How can energy cross a system boundary during a process?

    Respuesta

    As heat or work. Heat transferred to or work done on the system increases its energy; heat transferred from or work done by the system decreases it.

  261. Tarjeta 261

    Pregunta

    How does an endothermic reaction appear on an enthalpy diagram?

    Respuesta

    Products lie above reactants, so ΔH is positive.

  262. Tarjeta 262

    Pregunta

    How are heat gained by a system and heat lost by its surroundings related in an isolated setup?

    Respuesta

    qsystem = -qsurroundings.

  263. Tarjeta 263

    Pregunta

    In coffee-cup calorimetry, how is reaction heat related to solution heat?

    Respuesta

    qrxn = -qsolution when calorimeter heat is negligible and pressure is constant.

  264. Tarjeta 264

    Pregunta

    What heat is required to melt n moles at the melting point?

    Respuesta

    q = nΔHfus.

  265. Tarjeta 265

    Pregunta

    How does reversing a reaction change ΔH?

    Respuesta

    It reverses the sign of ΔH.

  266. Tarjeta 266

    Pregunta

    Why is breaking a bond endothermic?

    Respuesta

    Energy must be supplied to separate atoms against their bonding attraction.

  267. Tarjeta 267

    Pregunta

    How is ΔH°rxn calculated from standard enthalpies of formation?

    Respuesta

    ΣνΔHf°(products) − ΣνΔHf°(reactants).

  268. Tarjeta 268

    Pregunta

    How does multiplying an equation by 3 affect its ΔH?

    Respuesta

    Multiply ΔH by 3 because enthalpy change scales with reaction amount.

  269. Tarjeta 269

    Pregunta

    Why can an exothermic dissolution warm the solution?

    Respuesta

    The solution warms because forming solute–solvent attractions releases more energy than is absorbed in separating the original particles. The net potential-energy decrease raises particle kinetic energy and temperature.

  270. Tarjeta 270

    Pregunta

    Does an energy diagram's activation barrier determine ΔH?

    Respuesta

    No. ΔH depends on reactant and product energy levels, while the barrier controls kinetics.

  271. Tarjeta 271

    Pregunta

    Why does heat flow from a warmer object to a cooler object?

    Respuesta

    Energy transfers through collisions until their average kinetic energies, and therefore temperatures, equalize.

  272. Tarjeta 272

    Pregunta

    How much heat warms 100.0 g of water by 5.0°C?

    Respuesta

    2.1 kJ. Use q = (100.0 g)(4.184 J g^-1 °C^-1)(5.0°C).

  273. Tarjeta 273

    Pregunta

    How are the molar enthalpies of a phase change and its reverse related?

    Respuesta

    They have equal magnitudes and opposite signs, such as ΔHcond = -ΔHvap and ΔHfreeze = -ΔHfus.

  274. Tarjeta 274

    Pregunta

    How does doubling every coefficient in a thermochemical equation affect ΔH?

    Respuesta

    It doubles ΔH.

  275. Tarjeta 275

    Pregunta

    Why is forming a bond exothermic?

    Respuesta

    Atoms move to a lower-potential-energy bonded arrangement and release energy.

  276. Tarjeta 276

    Pregunta

    What formation equation defines ΔHf° for CO₂(g)?

    Respuesta

    C(s, graphite) + O₂(g) → CO₂(g), forming exactly one mole from elements in standard states.

  277. Tarjeta 277

    Pregunta

    What should happen to intermediate species when equations in a Hess’s law calculation are added?

    Respuesta

    They cancel, leaving the target overall reaction.

  278. Tarjeta 278

    Pregunta

    If the surroundings warm during a process, what is the likely sign of qsystem?

    Respuesta

    Negative; the system likely released heat to the surroundings.

  279. Tarjeta 279

    Pregunta

    For a profile with reactants at 40 kJ and products at 10 kJ, what is ΔH?

    Respuesta

    -30 kJ for the reaction as drawn.

  280. Tarjeta 280

    Pregunta

    Assuming no phase change, what determines the final temperature when two substances exchange heat in an insulated container?

    Respuesta

    Energy conservation: q_warm + q_cool = 0. Use each substance's mass, heat capacity, and initial temperature to solve for the common final temperature.

  281. Tarjeta 281

    Pregunta

    How would heat loss to the room affect an exothermic calorimetry result?

    Respuesta

    The observed temperature rise is too small, so the calculated magnitude of released heat is too low.

  282. Tarjeta 282

    Pregunta

    What heat expression covers warming a liquid without a phase change?

    Respuesta

    q = mcΔT, not nΔHphase.

  283. Tarjeta 283

    Pregunta

    If forming 1 mol of product has ΔH = -50 kJ mol^-1, what is q when 2 mol forms?

    Respuesta

    -100 kJ. Use q = nΔH = (2 mol)(-50 kJ mol^-1).

  284. Tarjeta 284

    Pregunta

    Breaking reactant bonds requires 500 kJ, and forming product bonds releases 650 kJ; what is the estimated ΔH?

    Respuesta

    -150 kJ, from 500 − 650.

  285. Tarjeta 285

    Pregunta

    For CO(g) + ½O₂(g) → CO₂(g), what is ΔH°rxn if ΔHf°[CO] = -110.5 and ΔHf°[CO₂] = -393.5 kJ mol^-1?

    Respuesta

    -283.0 kJ. Use -393.5 - [-110.5 + ½(0)], since ΔHf°[O₂(g)] = 0.

  286. Tarjeta 286

    Pregunta

    In a Hess’s law calculation, two valid steps have ΔH values +25 kJ and -60 kJ; what is the combined ΔH?

    Respuesta

    -35 kJ, provided the equations add to the target reaction.

  287. Tarjeta 287

    Pregunta

    Why is “bonds breaking releases energy” incorrect?

    Respuesta

    Bond breaking absorbs energy; the overall reaction releases energy only when forming new bonds releases more than breaking old bonds requires.

  288. Tarjeta 288

    Pregunta

    How would melting appear on an energy diagram?

    Respuesta

    The liquid lies above the solid, so ΔHfus is positive; the diagram represents a physical, endothermic change.

  289. Tarjeta 289

    Pregunta

    Can two objects at the same temperature exchange energy microscopically?

    Respuesta

    Yes, but their energy transfers balance, so there is no net heat flow.

  290. Tarjeta 290

    Pregunta

    Why must the calorimeter's heat capacity be included when it isn't negligible?

    Respuesta

    The apparatus can absorb or release heat, so include q_cal = C_calΔT in the energy balance: q_process + q_solution + q_cal = 0.

  291. Tarjeta 291

    Pregunta

    What makes chemical equilibrium dynamic?

    Respuesta

    Forward and reverse reactions continue at equal rates even though macroscopic concentrations stay constant.

  292. Tarjeta 292

    Pregunta

    For aA + bB ⇌ cC, what is the concentration-form expression for Q?

    Respuesta

    Q = [C]^c / ([A]^a[B]^b), using current rather than necessarily equilibrium concentrations.

  293. Tarjeta 293

    Pregunta

    What does K much greater than 1 indicate?

    Respuesta

    Products predominate at equilibrium, though K says nothing about reaction speed.

  294. Tarjeta 294

    Pregunta

    How does reversing a reaction change its equilibrium constant?

    Respuesta

    K becomes 1/K.

  295. Tarjeta 295

    Pregunta

    Can a reversible system reach equilibrium when it starts with only products?

    Respuesta

    Yes, if the reverse reaction is possible. The equilibrium composition depends on temperature, initial amounts, and volume or pressure.

  296. Tarjeta 296

    Pregunta

    How do Q and K predict reaction direction?

    Respuesta

    Q < K shifts forward, Q > K shifts reverse, and Q = K means equilibrium.

  297. Tarjeta 297

    Pregunta

    Which species are omitted from a heterogeneous equilibrium expression?

    Respuesta

    Pure solids and pure liquids because their activities are effectively constant.

  298. Tarjeta 298

    Pregunta

    How does increasing a dissolved reactant's concentration or a gaseous reactant's partial pressure affect equilibrium at constant temperature when other Q terms are initially unchanged?

    Respuesta

    It lowers Q relative to K, so the system shifts toward products until Q = K again. Changing the amount of a pure solid or liquid omitted from Q does not cause this shift while that pure phase remains present.

  299. Tarjeta 299

    Pregunta

    What does a flat concentration-time graph mean at equilibrium?

    Respuesta

    Each concentration is constant, not necessarily equal to the others.

  300. Tarjeta 300

    Pregunta

    For A ⇌ B in one fixed volume, a particulate model shows 16 A and 0 B initially, then 4 A and 12 B at equilibrium. What changed, what predominates, and what is Kc?

    Respuesta

    The net change was forward: 12 A particles became 12 B particles. B predominates at equilibrium, and Kc = [B]/[A] = 12/4 = 3.0 because both counts come from the same fixed volume.

  301. Tarjeta 301

    Pregunta

    What can Ksp tell you about a salt's solubility, and when can two Ksp values be compared directly?

    Respuesta

    Ksp > 1 indicates a soluble salt. For salts with the same dissolution stoichiometry, a larger Ksp generally means greater molar solubility; across different stoichiometries, calculate molar solubility before comparing.

  302. Tarjeta 302

    Pregunta

    What is the common-ion effect on solubility?

    Respuesta

    Adding an ion already in the dissolution equilibrium usually decreases the solid's molar solubility.

  303. Tarjeta 303

    Pregunta

    How does uniform dilution shift an aqueous equilibrium based on the stoichiometric powers in Q?

    Respuesta

    It shifts toward the side with the larger sum of stoichiometric coefficients for dissolved species included in Q. If the sums are equal, dilution causes no shift by this effect; pure solids and liquids remain omitted.

  304. Tarjeta 304

    Pregunta

    What happens if a reversible reaction starts with reactants only?

    Respuesta

    The forward rate is initially largest; products form, the reverse rate grows, and the rates eventually become equal.

  305. Tarjeta 305

    Pregunta

    What is the purpose of an ICE table?

    Respuesta

    To organize initial, change, and equilibrium concentrations using reaction stoichiometry.

  306. Tarjeta 306

    Pregunta

    Can a reaction with a very large K be slow?

    Respuesta

    Yes. K describes thermodynamic equilibrium position, while rate depends on kinetics and activation energy.

  307. Tarjeta 307

    Pregunta

    What happens to Q immediately after product concentration increases?

    Respuesta

    Q increases; if it rises above K, the reaction shifts toward reactants.

  308. Tarjeta 308

    Pregunta

    How does multiplying every reaction coefficient by 2 affect K?

    Respuesta

    The new equilibrium constant is K².

  309. Tarjeta 309

    Pregunta

    For A ⇌ B, Kc = 4.0 and initially [A] = 1.0 M and [B] = 0, what are the equilibrium concentrations?

    Respuesta

    [A] = 0.20 M and [B] = 0.80 M. Let x form: Kc = x/(1.0 − x) = 4.0, so x = 0.80 M.

  310. Tarjeta 310

    Pregunta

    What macroscopic properties stay constant at equilibrium?

    Respuesta

    Properties such as concentration, color, and pressure remain constant when external conditions are fixed.

  311. Tarjeta 311

    Pregunta

    How does decreasing volume shift a gaseous equilibrium?

    Respuesta

    Toward the side with fewer moles of gas, if the two sides have different gaseous mole counts.

  312. Tarjeta 312

    Pregunta

    For N₂ + 3H₂ ⇌ 2NH₃, what is Kc?

    Respuesta

    Kc = [NH₃]² / ([N₂][H₂]³).

  313. Tarjeta 313

    Pregunta

    For CaF₂(s) ⇌ Ca²⁺ + 2F⁻, how is Ksp written in terms of molar solubility s in pure water?

    Respuesta

    Ksp = s(2s)² = 4s³ because [Ca²⁺] = s and [F⁻] = 2s.

  314. Tarjeta 314

    Pregunta

    What does K much less than 1 indicate?

    Respuesta

    Reactants predominate at equilibrium.

  315. Tarjeta 315

    Pregunta

    How does decreasing a dissolved product's concentration or a gaseous product's partial pressure affect equilibrium when other Q terms are initially unchanged?

    Respuesta

    It lowers Q and drives a net forward reaction until equilibrium returns. Changing the amount of a pure solid or liquid omitted from Q does not cause this shift while that phase remains.

  316. Tarjeta 316

    Pregunta

    Does equilibrium mean the reaction has stopped?

    Respuesta

    No. Both directions continue, but equal rates produce no net macroscopic change.

  317. Tarjeta 317

    Pregunta

    Why does adding NaF reduce CaF₂ solubility?

    Respuesta

    The added F⁻ raises Qsp, shifting the dissolution equilibrium toward solid CaF₂.

  318. Tarjeta 318

    Pregunta

    For N₂ + 3H₂ ⇌ 2NH₃, what is Kp when P_N₂ = 0.50 atm, P_H₂ = 1.50 atm, and P_NH₃ = 0.25 atm?

    Respuesta

    0.037. Use Kp = (P_NH₃)²/[(P_N₂)(P_H₂)³] = (0.25)²/[(0.50)(1.50)³]. Use equilibrium partial pressures directly; Kc↔Kp conversion isn't assessed.

  319. Tarjeta 319

    Pregunta

    What happens to Q when a gaseous equilibrium mixture is compressed at constant temperature if products have fewer gas moles?

    Respuesta

    Q falls relative to K, so the reaction shifts toward products.

  320. Tarjeta 320

    Pregunta

    How do K and Q transform when a reaction is reversed, its coefficients are multiplied, or reactions are added?

    Respuesta

    They follow the same algebra: reversing takes the reciprocal, multiplying every coefficient by c raises the value to the power c, and adding reactions multiplies their K or Q values.

  321. Tarjeta 321

    Pregunta

    When is the small-x approximation acceptable?

    Respuesta

    When x is small relative to the initial concentration and the final result confirms the neglected change is suitably small.

  322. Tarjeta 322

    Pregunta

    What graph feature shows a disturbance followed by re-equilibration?

    Respuesta

    A sudden or gradual concentration change followed by new constant plateaus while rates return to equality.

  323. Tarjeta 323

    Pregunta

    If Q = 0.20 and K = 5.0, which direction is favored next?

    Respuesta

    Forward, because Q < K.

  324. Tarjeta 324

    Pregunta

    At equilibrium, are reactant and product concentrations equal?

    Respuesta

    Not necessarily. They are constant, while forward and reverse rates are equal.

  325. Tarjeta 325

    Pregunta

    CaF₂ has Ksp = 3.2 × 10^-11 in pure water; what is its molar solubility?

    Respuesta

    2.0 × 10^-4 M. If the molar solubility is s, then [Ca²⁺] = s, [F⁻] = 2s, and Ksp = 4s³.

  326. Tarjeta 326

    Pregunta

    For N₂ + 3H₂ ⇌ 2NH₃, how is Qp written?

    Respuesta

    Qp = (P_NH₃)²/[(P_N₂)(P_H₂)³], using the current partial pressures rather than necessarily equilibrium values.

  327. Tarjeta 327

    Pregunta

    How does heating shift an endothermic forward reaction?

    Respuesta

    Toward products, and K increases because temperature changes the equilibrium constant.

  328. Tarjeta 328

    Pregunta

    Why do both forward and reverse rates change as equilibrium is approached?

    Respuesta

    As reactant and product concentrations change, the collision frequencies for the two directions change until their rates match.

  329. Tarjeta 329

    Pregunta

    CaF₂ has Ksp = 3.2 × 10^-11. What is its molar solubility in 0.10 M NaF?

    Respuesta

    About 3.2 × 10^-9 M. With [F⁻] ≈ 0.10 M, Ksp = [Ca²⁺][F⁻]² gives s = (3.2 × 10^-11)/(0.10)². The common ion lowers solubility but does not change Ksp at constant temperature.

  330. Tarjeta 330

    Pregunta

    What concentration data must be used to calculate Kc?

    Respuesta

    Equilibrium concentrations, each raised to its stoichiometric coefficient and excluding pure solids and liquids.

  331. Tarjeta 331

    Pregunta

    What is a Brønsted–Lowry acid?

    Respuesta

    A proton donor.

  332. Tarjeta 332

    Pregunta

    How is pH defined?

    Respuesta

    pH = -log[H₃O⁺].

  333. Tarjeta 333

    Pregunta

    What is Ka for HA + H₂O ⇌ H₃O⁺ + A⁻?

    Respuesta

    Ka = [H₃O⁺][A⁻]/[HA].

  334. Tarjeta 334

    Pregunta

    How does stabilizing a base affect its basicity and the strength of its conjugate acid?

    Respuesta

    It makes the base weaker and its conjugate acid stronger. A more stable base is less willing to accept H⁺.

  335. Tarjeta 335

    Pregunta

    What is a Brønsted–Lowry base?

    Respuesta

    A proton acceptor.

  336. Tarjeta 336

    Pregunta

    At 25°C, what are Kw and the relationship between pH and pOH?

    Respuesta

    Kw = [H₃O⁺][OH⁻] = 1.0 × 10^-14. Taking negative logarithms gives pH + pOH = 14.00.

  337. Tarjeta 337

    Pregunta

    What is Kb for B + H₂O ⇌ BH⁺ + OH⁻?

    Respuesta

    Kb = [BH⁺][OH⁻]/[B].

  338. Tarjeta 338

    Pregunta

    Why can lowering pH increase the solubility of a salt containing a basic anion?

    Respuesta

    H₃O⁺ consumes the anion, pulling the dissolution equilibrium toward more dissolved ions.

  339. Tarjeta 339

    Pregunta

    What are conjugate acid–base pairs?

    Respuesta

    Species that differ by exactly one proton.

  340. Tarjeta 340

    Pregunta

    What is the pH of 1.0 × 10^-3 M HCl?

    Respuesta

    3.00, assuming complete dissociation and negligible water contribution.

  341. Tarjeta 341

    Pregunta

    How are pKa and pKb defined?

    Respuesta

    pKa = -log Ka, and pKb = -log Kb.

  342. Tarjeta 342

    Pregunta

    Why does acid strength increase across a row of comparable hydrides?

    Respuesta

    Increasing electronegativity stabilizes the conjugate base and polarizes the H–A bond.

  343. Tarjeta 343

    Pregunta

    What is an amphiprotic species?

    Respuesta

    A species that can donate or accept a proton, such as HCO₃⁻.

  344. Tarjeta 344

    Pregunta

    What amounts remain after a limited amount of strong base partially neutralizes weak acid HA?

    Respuesta

    Subtract the reacted moles from HA and form the same number of moles of A⁻. The result gives the remaining HA and formed A⁻ amounts before any equilibrium or buffer-pH calculation.

  345. Tarjeta 345

    Pregunta

    How are Ka, Kb, pKa, and pKb related for a conjugate pair at 25°C?

    Respuesta

    KaKb = Kw = 1.0 × 10^-14, and pKa + pKb = pKw = 14.00.

  346. Tarjeta 346

    Pregunta

    When does pH have little effect on a salt's solubility?

    Respuesta

    When neither dissolved ion reacts appreciably with H₃O⁺ or OH⁻.

  347. Tarjeta 347

    Pregunta

    How does H₂O act in HCl + H₂O → H₃O⁺ + Cl⁻ and in NH₃ + H₂O ⇌ NH₄⁺ + OH⁻?

    Respuesta

    It acts as a base in the first reaction by accepting H⁺, and as an acid in the second by donating H⁺.

  348. Tarjeta 348

    Pregunta

    After mixing weak base B with strong acid, what controls the final solution in the three stoichiometric regimes?

    Respuesta

    Excess B leaves a B/BH⁺ buffer; equimolar amounts leave BH⁺, so the solution is acidic; excess strong acid sets the pH from the remaining H₃O⁺.

  349. Tarjeta 349

    Pregunta

    What two components make a typical weak-acid buffer?

    Respuesta

    A weak acid and a significant amount of its conjugate base.

  350. Tarjeta 350

    Pregunta

    What do the successive half-equivalence pH values approximate in a diprotic weak-acid titration?

    Respuesta

    The first approximates pKa₁ and the second approximates pKa₂ because each conjugate pair has equal concentrations at its half-equivalence point.

  351. Tarjeta 351

    Pregunta

    Which acid is stronger, one with pKa 2 or pKa 5?

    Respuesta

    The acid with pKa 2; lower pKa means larger Ka.

  352. Tarjeta 352

    Pregunta

    What is the Henderson–Hasselbalch equation?

    Respuesta

    pH = pKa + log([A⁻]/[HA]).

  353. Tarjeta 353

    Pregunta

    Why are larger binary hydrides down a group often stronger acids?

    Respuesta

    The H–A bond becomes weaker as the central atom grows, so proton release is easier.

  354. Tarjeta 354

    Pregunta

    What mainly determines buffer capacity?

    Respuesta

    The concentrations of both members of the conjugate acid–base pair. Increasing both concentrations at a fixed ratio increases capacity without changing pH; capacity is best balanced for added acid and base when their concentrations are similar.

  355. Tarjeta 355

    Pregunta

    Why does acid increase CaCO₃ solubility?

    Respuesta

    H₃O⁺ converts CO₃²⁻ to HCO₃⁻ or carbonic acid species, reducing free carbonate and driving more CaCO₃ to dissolve.

  356. Tarjeta 356

    Pregunta

    What does pH < pKa imply for a weak-acid pair?

    Respuesta

    The protonated form HA predominates over A⁻.

  357. Tarjeta 357

    Pregunta

    What happens when stoichiometrically equal amounts of a monoprotic weak acid and strong base are mixed?

    Respuesta

    The weak acid is consumed to its conjugate base; at equivalence, the solution isn't a buffer containing both forms.

  358. Tarjeta 358

    Pregunta

    What is [H₃O⁺] when pH = 4.50?

    Respuesta

    3.2 × 10^-5 M, from [H₃O⁺] = 10^-pH.

  359. Tarjeta 359

    Pregunta

    What is the pH of 0.010 M Ba(OH)₂ at 25°C?

    Respuesta

    About 12.30. Complete dissociation gives [OH⁻] = 0.020 M, so pOH = 1.70. At 25°C, pH + pOH = 14.00, so pH = 12.30.

  360. Tarjeta 360

    Pregunta

    How does a buffer respond to a small amount of added strong acid?

    Respuesta

    Its conjugate base consumes H⁺, converting to the weak acid and limiting the pH change.

  361. Tarjeta 361

    Pregunta

    Why is the equivalence-point solution basic in a monoprotic weak-acid–strong-base titration?

    Respuesta

    The conjugate base produced at equivalence reacts with water to form OH⁻, so the pH is above neutral—above 7.00 at 25°C.

  362. Tarjeta 362

    Pregunta

    How is percent ionization calculated for a weak acid or weak base?

    Respuesta

    For HA, use ([H₃O⁺]equilibrium ÷ [HA]initial) × 100%. For B, use ([BH⁺]equilibrium ÷ [B]initial) × 100%, under the usual monoprotic setup.

  363. Tarjeta 363

    Pregunta

    When is Henderson–Hasselbalch useful for an initial buffer-pH calculation?

    Respuesta

    Use it when both members of a conjugate acid–base pair are present in meaningful amounts, including after in-scope stoichiometry creates a buffer. Calculating the pH change after acid or base is added to an existing buffer is outside this deck’s scope.

  364. Tarjeta 364

    Pregunta

    Why does adding oxygen atoms usually strengthen oxyacids with the same central atom?

    Respuesta

    Extra oxygens withdraw electron density and delocalize negative charge in the conjugate base.

  365. Tarjeta 365

    Pregunta

    A prepared buffer is accidentally diluted to twice its intended volume; what happens to its pH and capacity?

    Respuesta

    Its pH stays nearly the same, and its capacity per liter is halved because both component concentrations halve. The total neutralizing moles in the sample remain unchanged.

  366. Tarjeta 366

    Pregunta

    How does adding OH⁻ affect Mg(OH)₂ solubility?

    Respuesta

    It decreases solubility through the common-ion effect, shifting Mg(OH)₂(s) ⇌ Mg²⁺ + 2OH⁻ toward the solid.

  367. Tarjeta 367

    Pregunta

    A buffer has equal [A⁻] and [HA]; what is its pH?

    Respuesta

    pH = pKa because log(1) = 0.

  368. Tarjeta 368

    Pregunta

    How should a weak acid–strong base mixture be solved before equivalence?

    Respuesta

    First use mole stoichiometry; if both HA and A⁻ remain, use the resulting buffer relation.

  369. Tarjeta 369

    Pregunta

    Why can pure neutral water have a pH other than 7.00?

    Respuesta

    Kw changes with temperature. Neutrality means [H₃O⁺] = [OH⁻], while pH = 7.00 only when Kw = 1.0 × 10^-14 at 25°C.

  370. Tarjeta 370

    Pregunta

    25.0 mL of 0.200 M HCl is diluted to 100.0 mL; what is the pH?

    Respuesta

    1.301. Dilution gives [H₃O⁺] = (0.200 M)(25.0 mL)/(100.0 mL) = 0.0500 M, so pH = -log(0.0500).

  371. Tarjeta 371

    Pregunta

    How does a buffer respond to a small amount of added strong base?

    Respuesta

    The weak acid consumes OH⁻, forming conjugate base and water.

  372. Tarjeta 372

    Pregunta

    How do you find the final pH after mixing a strong acid and strong base at 25°C?

    Respuesta

    Use H₃O⁺ + OH⁻ → 2H₂O and compare their moles. Divide excess H₃O⁺ or OH⁻ by the total volume, then calculate pH or pOH from that excess concentration. Equal moles give pH 7.00 at 25°C.

  373. Tarjeta 373

    Pregunta

    What distinguishes acid strength from acid concentration?

    Respuesta

    Strength is the equilibrium tendency to donate H⁺, reflected by Ka or pKa; concentration is the amount of acid per solution volume.

  374. Tarjeta 374

    Pregunta

    If [A⁻]/[HA] = 10, how does pH compare with pKa?

    Respuesta

    pH = pKa + 1 because log 10 = 1.

  375. Tarjeta 375

    Pregunta

    Which conjugate base is more stable, one with localized or resonance-delocalized charge?

    Respuesta

    The resonance-delocalized conjugate base, which generally corresponds to the stronger acid.

  376. Tarjeta 376

    Pregunta

    Which 1.0 L buffer has greater capacity: 1.0 mol each of HA/A⁻ or 0.10 mol each at the same ratio?

    Respuesta

    The 1.0 mol pair; both have the same initial pH, but the larger amounts neutralize more added acid or base.

  377. Tarjeta 377

    Pregunta

    For BHX(s) ⇌ BH⁺ + X⁻, why can raising pH increase the salt's solubility?

    Respuesta

    OH⁻ consumes BH⁺ to form B and H₂O, so dissolution shifts right to replace BH⁺. This is a qualitative prediction, not a pH-dependent solubility calculation.

  378. Tarjeta 378

    Pregunta

    What does pH > pKa imply for a weak-acid pair?

    Respuesta

    The deprotonated form A⁻ predominates over HA.

  379. Tarjeta 379

    Pregunta

    For HA + B ⇌ A⁻ + BH⁺, which side is favored when pKa(HA) = 4 and pKa(BH⁺) = 9?

    Respuesta

    Products are favored. Proton transfer moves toward the weaker acid–base pair, and K ≈ 10^(9 − 4) = 10^5.

  380. Tarjeta 380

    Pregunta

    What is the pOH when [OH⁻] = 2.5 × 10^-4 M?

    Respuesta

    3.60, from -log(2.5 × 10^-4).

  381. Tarjeta 381

    Pregunta

    What is the pH of 0.100 M HA when Ka = 1.0 × 10^-5?

    Respuesta

    About 3.00. The ICE setup gives Ka = x²/(0.100 − x); x ≈ 1.0 × 10^-3 M, and the 1.0% change validates the approximation.

  382. Tarjeta 382

    Pregunta

    Why does a buffer fail after too much strong acid is added?

    Respuesta

    Its conjugate base is depleted, so added H⁺ is no longer consumed effectively.

  383. Tarjeta 383

    Pregunta

    What do two clear equivalence regions on an acid titration curve suggest?

    Respuesta

    At least two distinguishable titratable protons; on a clean ideal curve with exactly two equivalence regions, this is consistent with a diprotic acid.

  384. Tarjeta 384

    Pregunta

    A buffer has pKa 4.8 and [A⁻]/[HA] = 0.10; what is pH?

    Respuesta

    3.8, from 4.8 + log(0.10).

  385. Tarjeta 385

    Pregunta

    Why is HCl stronger than HF in water despite F being more electronegative?

    Respuesta

    The H–F bond is much stronger; bond strength dominates this down-group binary-acid comparison.

  386. Tarjeta 386

    Pregunta

    Why does percent ionization increase when a weak acid is diluted?

    Respuesta

    Dilution shifts ionization toward more particles, so a larger fraction ionizes even though [H₃O⁺] decreases.

  387. Tarjeta 387

    Pregunta

    A buffer contains more HA than A⁻. Which addition can it neutralize in greater amount: strong acid or strong base?

    Respuesta

    Strong base. The larger HA reserve consumes more added OH⁻; a buffer with more A⁻ than HA instead has greater capacity for added strong acid.

  388. Tarjeta 388

    Pregunta

    Why can removing a basic anion increase a salt's molar solubility without changing Ksp?

    Respuesta

    The equilibrium shifts to replace the consumed ion; Ksp remains fixed at the same temperature.

  389. Tarjeta 389

    Pregunta

    Why can an acid–base indicator change color as pH changes?

    Respuesta

    Its protonated and deprotonated forms have different colors or other observable properties, and their relative amounts change with pH.

  390. Tarjeta 390

    Pregunta

    What buffer results from mixing 1.0 mol HA with 0.40 mol OH⁻?

    Respuesta

    0.60 mol HA and 0.40 mol A⁻ remain, forming a buffer before any equilibrium calculation.

  391. Tarjeta 391

    Pregunta

    What is the pH of 0.200 M weak base B when Kb = 2.0 × 10^-5 at 25°C?

    Respuesta

    About 11.30. The ICE setup gives Kb = x²/(0.200 − x); x ≈ 2.0 × 10^-3 M OH⁻, and the 1.0% change validates the approximation.

  392. Tarjeta 392

    Pregunta

    Why does a weak acid alone not make an effective buffer?

    Respuesta

    It lacks a substantial conjugate-base reserve to consume added strong acid.

  393. Tarjeta 393

    Pregunta

    What controls pH after excess strong base passes equivalence?

    Respuesta

    The concentration of excess OH⁻ after accounting for reaction stoichiometry and total volume.

  394. Tarjeta 394

    Pregunta

    How should an indicator be chosen for a titration?

    Respuesta

    Its color-change range should fall within the steep pH change near the equivalence point.

  395. Tarjeta 395

    Pregunta

    How can a measured pH and known pKa give a conjugate-base/acid ratio?

    Respuesta

    Rearrange Henderson–Hasselbalch: [A⁻]/[HA] = 10^(pH − pKa).

  396. Tarjeta 396

    Pregunta

    Can a weak base and its conjugate acid form a buffer?

    Respuesta

    Yes, when both are present in significant amounts.

  397. Tarjeta 397

    Pregunta

    For equal-volume buffers with the same conjugate-base/acid ratio, how does adding the same amount of strong acid affect a more concentrated versus less concentrated buffer?

    Respuesta

    The concentrated buffer changes pH less because it has greater capacity.

  398. Tarjeta 398

    Pregunta

    How does equivalence-point pH compare for strong acid–strong base, weak acid–strong base, and weak base–strong acid titrations at 25°C?

    Respuesta

    Strong acid–strong base: pH 7.00. Weak acid–strong base: above 7.00 because the conjugate base reacts with water. Weak base–strong acid: below 7.00 because the conjugate acid reacts with water.

  399. Tarjeta 399

    Pregunta

    Why should mole ratios replace concentration ratios after mixing buffer solutions?

    Respuesta

    Both components share the same final volume, so that volume cancels in [A⁻]/[HA].

  400. Tarjeta 400

    Pregunta

    How does adding a little strong acid change a buffer's conjugate-base and conjugate-acid amounts?

    Respuesta

    The conjugate base decreases and its conjugate acid increases by the amount of strong acid consumed.

  401. Tarjeta 401

    Pregunta

    What does entropy measure qualitatively?

    Respuesta

    The dispersal of matter and energy among available microstates.

  402. Tarjeta 402

    Pregunta

    How is standard reaction entropy calculated?

    Respuesta

    ΔS°rxn = ΣνS°(products) − ΣνS°(reactants).

  403. Tarjeta 403

    Pregunta

    What equation gives ΔG° from ΔH° and ΔS°, and what standard states do the degree symbols assume?

    Respuesta

    ΔG° = ΔH° − TΔS°. The standard states are pure substances, 1.0 M solutions, and gases at 1 atm or 1 bar; T is in kelvins and energy units must match.

  404. Tarjeta 404

    Pregunta

    Does thermodynamic favorability guarantee a fast reaction?

    Respuesta

    No. A favorable reaction can be slow when its activation barrier is large.

  405. Tarjeta 405

    Pregunta

    What is ΔG at equilibrium?

    Respuesta

    Zero under the current conditions because there is no net driving force.

  406. Tarjeta 406

    Pregunta

    Why can an endothermic dissolution still be thermodynamically favorable?

    Respuesta

    A sufficiently positive entropy change can make TΔS exceed positive ΔH, giving negative ΔG.

  407. Tarjeta 407

    Pregunta

    How can an unfavorable reaction be driven by a favorable one?

    Respuesta

    Couple them so their equations and ΔG values add to a negative overall ΔG.

  408. Tarjeta 408

    Pregunta

    Where does oxidation occur in every electrochemical cell?

    Respuesta

    At the anode.

  409. Tarjeta 409

    Pregunta

    How are standard cell potential and standard free energy related?

    Respuesta

    ΔG° = -nFE°cell.

  410. Tarjeta 410

    Pregunta

    What equation gives cell potential under nonstandard conditions?

    Respuesta

    E = E° − (RT/nF) ln Q. When Q = 1, ln Q = 0, so E = E°.

  411. Tarjeta 411

    Pregunta

    How is electrical charge related to current and time?

    Respuesta

    q = It.

  412. Tarjeta 412

    Pregunta

    Which phase has greater molar entropy, liquid water or ice at the same temperature?

    Respuesta

    Liquid water because its molecules have more accessible arrangements and motion.

  413. Tarjeta 413

    Pregunta

    Do elements in their standard states have zero standard molar entropy?

    Respuesta

    No. Their ΔHf° is zero, but their absolute S° values are positive above 0 K.

  414. Tarjeta 414

    Pregunta

    How do the four ΔH° and ΔS° sign combinations determine thermodynamic favorability across temperature?

    Respuesta

    ΔH° < 0 and ΔS° > 0 is favorable at every temperature; ΔH° > 0 and ΔS° < 0 is thermodynamically unfavored at every temperature. If both are positive, favorability requires high temperature; if both are negative, it requires low temperature.

  415. Tarjeta 415

    Pregunta

    What does it indicate when a thermodynamically favored process does not occur at a measurable rate?

    Respuesta

    It is under kinetic control, commonly because of a high activation energy; no measurable reaction does not mean the system is at equilibrium.

  416. Tarjeta 416

    Pregunta

    How are ΔG° and K related?

    Respuesta

    ΔG° = -RT ln K.

  417. Tarjeta 417

    Pregunta

    What two contributions compete in dissolving an ionic solid?

    Respuesta

    Enthalpy changes from separating and solvating particles, and entropy changes from their new dispersal and solvent organization.

  418. Tarjeta 418

    Pregunta

    What must cancel when coupled reactions are added?

    Respuesta

    Shared intermediates, leaving the desired net reaction.

  419. Tarjeta 419

    Pregunta

    Where does reduction occur in every electrochemical cell?

    Respuesta

    At the cathode.

  420. Tarjeta 420

    Pregunta

    What sign of E°cell indicates a favorable standard galvanic reaction?

    Respuesta

    Positive E°cell, corresponding to negative ΔG°.

  421. Tarjeta 421

    Pregunta

    If Q increases for a galvanic reaction, how does E change at fixed temperature?

    Respuesta

    E decreases according to the Nernst equation. Le Châtelier's principle does not apply to an operating cell away from equilibrium; use Q and Nernst reasoning instead.

  422. Tarjeta 422

    Pregunta

    How are moles of electrons found from charge?

    Respuesta

    Moles e⁻ = q/F, where F ≈ 96485 C mol^-1 e⁻.

  423. Tarjeta 423

    Pregunta

    How does producing more gas particles usually affect system entropy?

    Respuesta

    It increases entropy because the particles have more positional microstates.

  424. Tarjeta 424

    Pregunta

    Can a dissolution with negative ΔH be unfavorable?

    Respuesta

    Yes. A sufficiently negative entropy change at the stated temperature can make ΔG positive.

  425. Tarjeta 425

    Pregunta

    When can a process with ΔH > 0 and ΔS > 0 become favorable?

    Respuesta

    At sufficiently high temperature, when TΔS exceeds ΔH.

  426. Tarjeta 426

    Pregunta

    How does a catalyst affect ΔG?

    Respuesta

    It does not change ΔG; it lowers the activation barrier for both directions.

  427. Tarjeta 427

    Pregunta

    For A → B, ΔGf°(A) = -50 kJ mol^-1 and ΔGf°(B) = -80 kJ mol^-1. What is ΔG°rxn?

    Respuesta

    -30 kJ mol^-1. Use ΣνΔGf°(products) − ΣνΔGf°(reactants) = -80 − (-50).

  428. Tarjeta 428

    Pregunta

    Why can dissolving a gas in a liquid have a negative entropy change?

    Respuesta

    Gas particles lose much of their translational freedom when confined and solvated in the liquid.

  429. Tarjeta 429

    Pregunta

    If coupled steps have ΔG values +20 kJ and -35 kJ, what is overall ΔG?

    Respuesta

    -15 kJ, so the combined process is thermodynamically favorable under those conditions.

  430. Tarjeta 430

    Pregunta

    What role does each half-cell solution play in an electrochemical cell?

    Respuesta

    It supplies dissolved redox species at an electrode interface and carries ions within its compartment. Separate compartments prevent direct mixing while the external circuit and salt bridge connect the half-cells.

  431. Tarjeta 431

    Pregunta

    How is E°cell found from standard reduction potentials?

    Respuesta

    E°cell = E°cathode − E°anode, using both tabulated values as reductions.

  432. Tarjeta 432

    Pregunta

    How does a cell's potential magnitude change as Q approaches or moves away from K, and what is E at equilibrium?

    Respuesta

    |E| falls toward zero as Q approaches K and grows as the system moves farther from equilibrium. At equilibrium, Q = K and E = 0.

  433. Tarjeta 433

    Pregunta

    How many moles of electrons pass when 1.93 × 10^5 C flows?

    Respuesta

    2.00 mol e⁻, from q/F.

  434. Tarjeta 434

    Pregunta

    How does a salt bridge maintain charge balance in a galvanic cell?

    Respuesta

    Anions migrate toward the anode compartment and cations toward the cathode compartment, countering the net charge imbalances created by the two half-reactions.

  435. Tarjeta 435

    Pregunta

    Why does raising a substance's temperature generally increase its entropy?

    Respuesta

    Energy spreads across more accessible particle energy states, increasing the number of possible microscopic arrangements.

  436. Tarjeta 436

    Pregunta

    When can a process with ΔH < 0 and ΔS < 0 be favorable?

    Respuesta

    At sufficiently low temperature, where the unfavorable -TΔS term is small.

  437. Tarjeta 437

    Pregunta

    Why can diamond persist even though graphite is more stable at standard conditions?

    Respuesta

    Conversion has a large activation barrier, so diamond is kinetically persistent.

  438. Tarjeta 438

    Pregunta

    What do the external circuit and measuring device do in an electrochemical cell?

    Respuesta

    The circuit carries electrons from anode to cathode; a voltmeter measures potential difference, while an ammeter in series measures current.

  439. Tarjeta 439

    Pregunta

    At constant temperature, how does increasing the volume available to a gas affect its entropy?

    Respuesta

    Entropy increases because the gas particles can occupy more positions in the larger space, so more microstates are accessible.

  440. Tarjeta 440

    Pregunta

    How does reversing one coupled reaction affect its ΔG?

    Respuesta

    It reverses the sign of that reaction's ΔG.

  441. Tarjeta 441

    Pregunta

    Why is n required in ΔG° = -nFE°?

    Respuesta

    It is the moles of electrons transferred per balanced reaction, linking charge flow to reaction extent.

  442. Tarjeta 442

    Pregunta

    What makes an electrolytic cell operate?

    Respuesta

    An external power source drives a thermodynamically unfavorable redox reaction; oxidation still occurs at the anode and reduction at the cathode.

  443. Tarjeta 443

    Pregunta

    In an Mⁿ⁺/M concentration cell, which half-cell is the anode: the dilute or concentrated ion solution?

    Respuesta

    The dilute half-cell. Oxidation produces Mⁿ⁺ there, while reduction consumes Mⁿ⁺ in the concentrated half-cell, so electrons flow from dilute to concentrated as the concentrations move toward equality.

  444. Tarjeta 444

    Pregunta

    How is deposited metal mass found from current and time?

    Respuesta

    Find q = It, convert q/F to moles e⁻, use the half-reaction ratio to moles metal, then multiply by molar mass.

  445. Tarjeta 445

    Pregunta

    Given product S° total 500 J mol^-1 K^-1 and reactant total 420 J mol^-1 K^-1, what is ΔS°?

    Respuesta

    +80 J mol^-1 K^-1.

  446. Tarjeta 446

    Pregunta

    How do electrode masses change in a Zn–Cu galvanic cell?

    Respuesta

    The Zn anode loses mass as Zn → Zn²⁺ + 2e⁻, while the Cu cathode gains mass as Cu²⁺ + 2e⁻ → Cu.

  447. Tarjeta 447

    Pregunta

    What is ΔG° when ΔH° = 50 kJ mol^-1, ΔS° = 0.200 kJ mol^-1 K^-1, and T = 300 K?

    Respuesta

    -10 kJ mol^-1, from ΔG° = 50 − (300)(0.200).

  448. Tarjeta 448

    Pregunta

    Why can temperature change a solid's solubility?

    Respuesta

    Temperature changes the balance of ΔH and TΔS, so it changes the free energy of dissolution and the equilibrium constant.

  449. Tarjeta 449

    Pregunta

    What does the size of ΔG° relative to RT imply about K?

    Respuesta

    ΔG° near zero gives K near 1. When |ΔG°| is much larger than RT, K is far from 1: negative ΔG° gives K ≫ 1, while positive ΔG° gives K ≪ 1.

  450. Tarjeta 450

    Pregunta

    Bubbles form at an inert cathode in acidic solution; which half-reaction can explain them?

    Respuesta

    2H⁺ + 2e⁻ → H₂(g). Gas evolution at the cathode can be direct evidence of reduction.

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Advanced High School Chemistry Flashcards: Complete 9-Part Course Review

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