Structure and Bonding Flashcards

Definitions (80 cards)

1
Q
  • protons and neutrons
  • electron cloud
  • mass (nucleus)
  • volume (electron)
A

Atomic Structure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

two or more forms of the same element that contain equal numbers of protons but different numbers of neutrons

A

Isotopes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

electron location unknown but electron density is known

A

Quantum Mechanical Model

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

electron will be in a certain region of space (orbital) at a given instant

A

Electron Density

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Electrons do not circle around the nucleus in fixed orbits but rather,
in ________.

A

Orbitals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Each orbital has a characteristic _____and ____ (energy).

A

Shape and Size

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

used to described orbitals

A

Quantum Numbers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

lowest-energy orbitals fill up first

A

Aufbau Principle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

If two or more empty orbitals of equal energy are available, one electron occupies each with spins parallel until all orbitals are half-full,

A

Hund’s Rule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Only two electrons can occupy an orbital, and they must
have opposite spins

A

Pauli’ Exclusion Principle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

there is a limit to the precision with which certain pairs of physical properties can be simultaneously known

A

Heisenberg’s Uncertainty Principle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Electron BELOW the outermost shell

A

Core Electrons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Electrons IN the outermost shell

A

Valence Electrons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

An attractive force between two ions or between two atoms

A

Chemical bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Why do chemical bonds form?

A

more stable and lower in energy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How do chemical bonds form?

A

Octet Rule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Chemistry of main-group elements is governed by their tendency to
take on the electron configuration of the nearest noble gas.

A

Octet Rule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Attractive forces between opposite charges

A

Electrostatic Attraction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

formed in electrostatic attraction
formed in transfer of electrons
reaction of metals with nonmetals

A

Ionic Bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Compounds formed by ionic bonds

A

Ionic Compound

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Bond formed as a result of sharing electrons between two nuclei

A

Covalent Bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Compounds formed by covalent bonds

A

Molecular compounds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Measure of the ability of an atom to pull the bonding electrons toward itself

A

Electronegativity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

covalent bond between atoms with SAME electronegativity

A

Nonpolar covalent bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
covalent bond between atoms with DIFFERENT ELECTRONEGATIVITIES
Polar covalent bond
26
< 0.4
pure covalent
27
between 0.4 and 1.8
Polar covalent
28
> 1.8
ionic
29
a pair of equal and oppositely charged poles separated by a DISTANCE
Dipole
30
Measure of Dipole
Dipole moment
31
magnitude of the charge on either atom x distance between the two charges
Dipole moment
32
electron-dot structures
Lewis Structures
33
line-bond structures
Kekule Structures
34
not an actual charge, used for bookkeeping of electrons
Formal charge
35
charge if each bonding electron pair in the molecule were shared equally between atoms
Formal Charge
36
Difference VE when it is not bonded and VE when it is bonded
Formal Charge
37
OMITTING OF THE COVALENT bonds and listing atoms bonded to a particular carbon (or nitrogen or oxygen) next toit (with a subscript if there is more than one of a particular atom)
Condensed structures
38
C atoms aren't shown C atoms are assume in the lines H atoms aren't shown Atoms other than C and H are shown
Skeletal structures
39
Shows 3D shape
Perspective Drawing
40
Show bond angles accurately
Ball-and-Stick Model
41
Shows atoms in scale
Space-filling Model
42
Bond lies in the plane of the paper
Normal Bond
43
Bond extends backwards, away from the viewer
Dashed bond
44
Bond protudes forwards, toward the viewer
Wedged bond
45
Geometry based on arrangement of atoms in a molecule + defined by bond angles
Molecular Geometry
46
Geometry based on valence electron pairs around a central atom + Defined by bond angles
Electron pair geometry
47
A model for the prediction of molecular geometry based on the MINIMIZATION OF ELECTRON REPULSION between regions of eelctron density around an atom
Valence-Shell Electron-Pair Repulsion Model (VSEPR)
48
The best arrangement of a given number of electron pairs (bonding and nonbonding) is the one that minimizes the repulsions among them.
Valence-Shell Electron-Pair Repulsion Model (VSEPR)
49
Without lone pairs:
Electron Pair Geometry and Molecular Geometry is equal
50
assumes that the electrons in a molecule occupy OVERLAPPING atomic orbitals of the individual atoms
Valence Bond Theory
51
Assumes the formation of molecular orbitals from the atomic orbitals
Molecular Orbital Theory
52
How is covalent bonds formed?
When atomic orbitals on neighboring atoms overlap one another
53
head-on overlap of atomic orbitals; stronger
Sigma σ
54
sideway overlap of atomic orbitals; weaker
PI BONDS (π)
55
atomic orbitals obtained when TWO OR MORE NONEQUIVALENT ORBITALS of the SAME ATOM combine for covalent bond formation
Hybrid Orbitals
56
Produces the molecular geometry of the molecule.
Hybridization
57
The greater the electron density in the gregion of orbital overlap
The stronger and shorter the bond
58
As s character increases, bond angle _______
Increases
59
Describes a region of space in a molecule where electrons are most likely to be found
Molecular Orbital
60
2 ways to combine atomic orbitals into molecular orbitals
Additive and Subtractive
61
2 ways to combine atomic orbitals into molecular orbitals ? - Lower energy, bonding molecular oribtal
Additive
62
2 ways to combine atomic orbitals into molecular orbitals ? - higher energy, antibonding molecular orbital
Subtractive
63
occurs when an electron is shared by more than 2 atoms with π bonds (p orbitals)
π ELECTRON DELOCALIZATION
64
Structures are represented by resonance contributors
π ELECTRON DELOCALIZATION
65
Some substances can’t be represented by a single line-bond structure and must be considered as a resonance hybrid of two or more structures.
Resonance
66
two individual line-bond structures
Resonance forms
67
indicated by the double- headed arrow between them.
Special Resonance Relationship
68
What is the different between resonance forms?
Placement of the π BOND and NONBONDING VALENCE ELECTRONS
69
single unchanging structure
Resonance Hybrid
70
two individual forms and has characteristics of both
Resonance Hybrid
71
Between resonance forms
Double headed arrow
72
Movement of electrons
Curly Arrow
73
From electron-rich species
Tail
74
To electron-deficient specials
Head
75
Double bonds separated by single bonds
Conjugation
76
Refers to a system that has a p orbital adjacent to a π bond allowing delocalization of π electrons
Conjugation
77
Compounds with isolated double bonds (___________)
Higher energy
78
Special kind of conjugation and cyclic unsaturated molecules with unusual stability
Aromaticity
79
Originally used to classify benzene and its derivatives because many of them have distinctive odors
Aromaticity
80