Quiz #1 Flashcards

1
Q

Definition of molecular orbital

A

Combined atomic orbitals

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2
Q

Molecular orbitals

A

Cannot be created or destroyed

Arranged in order of increasing energies

Filled according to Aufbau, Pauli, and Hund rules

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3
Q

Which orbital has the highest energy, bonding/sigma or antiboding/sigma*

A

The antibonding/sigma* orbital

This is why the bonding/sigma orbital is favored, it has the lower energy

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4
Q

Bonding angle and geometry for sp3 orbitals

A

~109.5, tetrahedral

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5
Q

Bonding angle and geometry for sp2 orbitals

A

120, trigonal planar

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6
Q

Bonding angle and geometry for sp orbitals

A

180, linear

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7
Q

4 regions of electron density

A

sp3 hybridized bonding orbital

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8
Q

3 regions of electron density

A

sp2 hybridized bonding orbital

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9
Q

2 regions of electron density

A

sp hybridized bonding orbital

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10
Q

Formal charge equation

A

of valence electrons in the neutral unbonded atom – (the # of non-bonding electrons + the # of bonds)

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11
Q

Rules for arrow pushing

A
  1. Double headed curved arrow means two electrons are moving
  2. Arrows move from electron rich regions to electron poor regions, never the other way around
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12
Q

Steps to drawing resonance structutes

A
  1. Convert any lone pairs to pi bonds
  2. Convert any pi bonds to lone pairs
  3. Convert any pi bonds to other pi bonds

Remember the two commandments: thou shalt not break single bonds, and thou shalt not break the octet rule for second row elements

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13
Q

Patters to drawing resonance structures

A
  1. Lone pair next to pi bond
  2. Lone pair next to C+
  3. Pi bond next to C+
  4. Pi bond between two atoms, one of which is electronegative
  5. Pi bonds around in a ring
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14
Q

What makes a valid resonance structure?

A
  1. Must have the same # of valence electrons
  2. Must be a valid Lewis structure
  3. Must have the same # of paired and unpaired electrons
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15
Q

Criteria for more favored resonance structures

A

Most filled valence shells and complete octets

Most covalent bonds

Fewest formal charges

Optimal charge distribution, with the negative charge on the most electronegative atom

Note that equally favored structures contribute equally to the resonance hybrid

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