12-15 Flashcards

(60 cards)

1
Q
  1. What is bond energy?
A

Bond energy is the amount of energy required to break one mole of a bond in a compound in the gas state, with the bonding electrons shared equally between the atoms (homolytically).

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2
Q
  1. How can the enthalpy of a reaction be estimated using bond energies?
A

The enthalpy change (ΔH) of a reaction can be estimated by summing the bond energies of the bonds broken (endothermic) and subtracting the bond energies of the bonds formed (exothermic). The formula is:
ΔH = Σ (bonds broken) - Σ (bonds formed).

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3
Q
  1. What is the general trend of bond energy in covalent bonds?
A

Generally, the more electrons two atoms share, the stronger the bond. For example, C≡C (837 kJ/mol) is stronger than C=C (611 kJ/mol) and C−C (347 kJ/mol).

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4
Q
  1. What happens to bond strength as bond length increases?
A

As bond length increases, bond strength typically decreases. For example, C≡N (116 pm) is shorter and stronger than C=N (128 pm), which in turn is shorter and stronger than C−N (147 pm).

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5
Q
  1. What factors affect the actual bond energy in a molecule?
A

The actual bond energy depends on the surrounding atoms and other environmental factors in the molecule, making average bond energies a useful but sometimes imperfect estimation.

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6
Q
  1. Why is bond breaking endothermic and bond making exothermic?
A

Breaking bonds requires energy, so it is endothermic, and making bonds releases energy, so it is exothermic.

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7
Q
  1. How does the bond energy of halogens change down the group?
A

As you go down the halogen group, bond energy decreases. For example, F−F has a higher bond energy (144 pm) than Br−Br (228 pm).

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8
Q
  1. What is bond length and how is it measured?
A

Bond length is the distance between the nuclei of two bonded atoms, and it is usually measured in picometers (pm).

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9
Q
  1. How does bond length change across a period and down a group?
A

Across a period, bond length decreases due to increasing nuclear charge, and down a group, bond length increases due to larger atomic radii.

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10
Q
  1. What are the basic shapes predicted by VSEPR theory?
A

VSEPR theory predicts five basic shapes based on the arrangement of electron pairs: linear, trigonal planar, tetrahedral, trigonal bipyramidal, and octahedral.

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11
Q
  1. What is the difference between electron group geometry and molecular geometry?
A

Electron group geometry describes the spatial arrangement of all electron pairs around a central atom, while molecular geometry only considers the arrangement of atoms, excluding lone pairs.

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12
Q
  1. What is the AXmEn designation in VSEPR theory?
A

In the AXmEn designation, ‘A’ represents the central atom, ‘X’ represents the bonded atoms, ‘E’ represents the lone pairs, and ‘m’ and ‘n’ are integers representing the number of bonded atoms and lone pairs, respectively.

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13
Q
  1. How does the presence of lone pairs affect bond angles?
A

Lone pairs repel more strongly than bonding pairs, causing bond angles to decrease. For example, in a tetrahedral structure with lone pairs, the bond angle is less than the ideal 109.5°.

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14
Q
  1. What is a pyramidal molecular geometry?
A

Pyramidal geometry occurs when there are four electron groups around a central atom, and one is a lone pair, creating a triangular base pyramid shape.

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15
Q
  1. What is a bent molecular geometry?
A

A bent molecular geometry occurs when there are four electron groups around a central atom, and two are lone pairs, resulting in a bent shape with a bond angle less than 109.5°.

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16
Q
  1. How do you use bond energies to estimate ΔH for the reaction: H2(g) + O2(g) → H2O2(g)?
A

The ΔH is estimated by summing the bond energies of the bonds broken (+936 kJ) and subtracting the bond energies of the bonds formed (-1070 kJ), resulting in ΔHrxn = -136 kJ.

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17
Q
  1. What are the key concepts of metallic bonding?
A

In metallic bonding, metal atoms release their valence electrons to form a “sea of electrons,” which are delocalized and free to move throughout the metal lattice. This creates strong attractions between the cations and the delocalized electrons.

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18
Q
  1. What is the significance of bond vibrations in IR spectroscopy?
A

Bond vibrations, such as stretching and bending, can be detected using infrared (IR) spectroscopy, as different bonds absorb IR radiation at characteristic frequencies based on their bond strength.

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19
Q
  1. What is a resonance structure and how does it affect electron geometry?
A

Resonance structures represent different possible arrangements of electron pairs in a molecule. However, the overall electron geometry of the central atom remains the same when considering the resonance hybrid.

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20
Q
  1. How do multiple bonds (double and triple bonds) affect molecular geometry?
A

In VSEPR theory, multiple bonds (double or triple) are treated as single electron groups. Therefore, the molecular geometry is determined by the total number of electron groups, not by the number of bonds within each group.

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21
Q
  1. Definition of Bond Energy
A
  • The energy required to break one mole of a bond in a compound, typically in the gas state and homolytically, where each atom receives half of the bonding electrons.
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22
Q
  1. General Trends in Bond Energies
A
  • The more electrons two atoms share, the stronger the covalent bond. Shorter bonds are typically stronger (e.g., C≡C > C=C > C−C).
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23
Q
  1. Using Bond Energies to Estimate ∆H°rxn
A
  • ∆H°rxn is estimated by comparing the energy required to break bonds (endothermic) to the energy released by forming new bonds (exothermic).
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24
Q
  1. Bond Breaking and Making in Terms of ∆H
A
  • Bond breaking is endothermic (positive ∆H), and bond making is exothermic (negative ∆H).
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25
5. Example of Calculating ∆H°rxn
* For the reaction CH₄ + Cl₂ → CH₃Cl + HCl: * Bond breaking: +657 kJ * Bond making: −770 kJ * ∆H°rxn = −113 kJ
26
Bond Length
The distance between the nuclei of bonded atoms. It depends on surrounding atoms, and average bond lengths are used for estimation
27
Trends in Bond Lengths
Bonds tend to be shorter with more electron sharing (e.g., C≡C < C=C < C−C). Bond lengths decrease across a period and increase down a group.
28
Bond Vibration
Bonds are not static and can vibrate in different motions, such as symmetrical stretching, anti-symmetrical stretching, and more.
29
Infrared Spectroscopy and Bond Vibration
IR spectroscopy detects bond vibrations. The vibrational energy depends on bond strength and is measured as a wavenumber.
30
10. Electron Sea Model in Metallic Bonds
Metals release their valence electrons to form a “sea” of delocalized electrons, which bonds the metal cations.
31
Valence-Shell Electron-Pair Repulsion (VSEPR) Theory
Predicts molecular geometry by minimizing electrostatic repulsion between electron groups.
32
Electron Group Geometry vs. Molecular Geometry
Electron group geometry refers to the spatial arrangement of electron groups, while molecular geometry refers to the arrangement of atomic nuclei.
33
Effect of Lone Pairs on Molecular Geometry
Lone pairs occupy more space than bonding pairs, distorting bond angles in a molecule.
34
Basic Electron Group Arrangements
There are five basic arrangements: linear, trigonal planar, tetrahedral, trigonal bipyramidal, and octahedral.
35
AXmEn Notation in VSEPR
This notation helps describe the structure of a molecule, where A represents the central atom, X represents bonded atoms, and E represents lone pairs.
36
Linear Geometry
Occurs when there are two electron groups around the central atom, such as in CO₂.
37
Trigonal Planar Geometry
Occurs when there are three electron groups around the central atom, with a bond angle of 120°, such as in BF₃.
38
Pyramidal Shape
Occurs when there are four electron groups but one is a lone pair, leading to a pyramidal shape, such as in NH₃.
39
Tetrahedral Geometry
Occurs with four electron groups around the central atom, forming bond angles of 109.5°, such as in CH₄.
40
Bent Geometry
When a molecule has two lone pairs and two bonded atoms, the geometry is bent, such as in H₂O, with bond angles smaller than 109.5°.
41
What does VSEPR theory predict about molecular geometry?
VSEPR (Valence-shell electron-pair repulsion) theory predicts molecular geometry by arranging electron pairs to minimize electrostatic repulsions.
42
How do lone pairs affect molecular geometry?
Lone pairs take up more space than bonding pairs, causing bond angles to be smaller than expected in molecules like bent or trigonal pyramidal shapes.
43
What is electron group geometry?
Electron group geometry refers to the arrangement of electron groups (both bonding and lone pairs) around a central atom.
44
How does VSEPR theory treat double and triple bonds?
VSEPR theory treats double and triple bonds as a single electron group, just like single bonds.
45
What is the AXmEn notation in VSEPR theory?
AXmEn notation is a system where A represents the central atom, X represents bonded atoms, and E represents nonbonding electron groups (lone pairs), with m and n being integers.
46
What molecular geometry results from a tetrahedral arrangement with one lone pair?
A tetrahedral arrangement with one lone pair results in a trigonal pyramidal molecular geometry.
47
What is the bond angle in a tetrahedral geometry?
The bond angle in a tetrahedral geometry is approximately 109.5°.
48
How does the seesaw shape arise in VSEPR theory?
The seesaw shape occurs when there are five electron groups around a central atom, with one being a lone pair, causing a distortion from the ideal trigonal bipyramidal shape.
49
What is the molecular geometry of a molecule with five electron groups and two lone pairs?
The molecular geometry is T-shaped when there are five electron groups and two lone pairs around the central atom.
50
What bond angle is typical for a linear molecular geometry with two electron groups?
The bond angle in a linear geometry is 180°.
51
How does the square pyramidal shape form in VSEPR theory
A square pyramidal shape forms when there are six electron groups around the central atom, with one being a lone pair.
52
What is the molecular geometry of a molecule with six electron groups and two lone pairs?
The molecular geometry is square planar when there are six electron groups and two lone pairs around the central atom.
53
What does the presence of lone pairs do to bond angles?
Lone pairs reduce bond angles by repelling bonding electron pairs more strongly than bonding pairs repel each other.
54
How do polar bonds contribute to molecular polarity?
Polar bonds occur due to differences in electronegativity between atoms, creating dipole moments. The overall polarity of a molecule depends on the vector sum of its bond dipoles.
55
How do London dispersion forces arise?
London dispersion forces arise from temporary fluctuations in electron distribution, creating short-lived dipoles that induce dipoles in neighboring molecules
56
What are the criteria for a molecule to be polar?
A molecule is polar if it has polar bonds and the bond dipoles do not cancel out, resulting in a net dipole moment.
57
What factors affect the strength of London dispersion forces?
The strength of London dispersion forces depends on the polarizability of the electron cloud (which increases with molar mass) and the shape of the molecule (more surface area increases interactions).
58
18. What is the effect of dipole-dipole interactions on boiling and melting points?
Dipole-dipole interactions increase the boiling and melting points of polar molecules compared to nonpolar molecules of similar size.
59
How does hydrogen bonding affect the properties of a substance?
Hydrogen bonding, which occurs between molecules containing highly electronegative atoms like N, O, or F bonded to hydrogen, significantly raises the boiling and melting points due to the strong dipole interactions.
60
What is ion-dipole attraction, and why is it important?
Ion-dipole attraction occurs between an ion and the dipole of a polar molecule, which is crucial for the solubility of ionic compounds in water.