Chp 2 Flashcards

(20 cards)

1
Q

What are the recommended practice problems from Klein in Chapter 2?

A

2.1, 2.5, 2.8 (a-f), 2.10, 2.12, 2.14, 2.16, 2.21, 2.23, 2.25, 2.26, 2.32, 2.37, 2.40, 2.43, 2.52, 2.54, 2.58, 2.62 and 2.64

These problems are intended to reinforce concepts related to molecular representations.

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2
Q

What are the characteristics of condensed structures?

A

No bonds are shown but there is still structural information

Condensed structures provide a simplified view of molecular connectivity.

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3
Q

In bond-line structures, how are carbon atoms represented?

A

Carbon atoms are not labeled; assumed at every corner or endpoint

This simplifies the representation of organic molecules.

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4
Q

What is the maximum number of bonds that can be drawn to a carbon atom?

A

4 bonds

Exceeding this would violate the tetravalency of carbon.

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5
Q

What is the bond angle for an sp² hybridized carbon?

A

120 degrees

This geometry is typical for trigonal planar arrangements.

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6
Q

What are functional groups?

A

Characteristic groups of atoms/bonds that possess a predictable chemistry

Functional groups determine the chemical reactivity of molecules.

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7
Q

What does IR spectroscopy utilize to cause transitions in vibrational energy levels?

A

Photons of a certain energy

This technique helps identify functional groups based on their vibrational modes.

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8
Q

What does formal charge impact in molecules?

A

Stability and reactivity

Understanding formal charge is crucial for predicting molecular behavior.

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9
Q

What is the formula for calculating formal charge?

A

Formal charge = # normal valence electrons – [electrons in lone pair + ½ of bonding electrons]

This formula helps identify the charge on atoms in a molecule.

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10
Q

What is a carbocation?

A

A positively charged carbon atom

This occurs when a carbon has three bonds instead of four.

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11
Q

What is a carbanion?

A

A negatively charged carbon atom

This occurs when a carbon has three bonds and carries a -1 charge.

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12
Q

How are 3D bond-line structures represented on paper?

A

Using dashed and solid wedges

This indicates groups that point into or out of the paper.

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13
Q

What is resonance in chemistry?

A

A method representing the distribution of electrons throughout a molecule’s π orbitals

Resonance structures illustrate multiple valid electron arrangements.

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14
Q

What is resonance stabilization?

A

The spreading of charge that stabilizes a molecule

This occurs when charge delocalization reduces the energy of a molecule.

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15
Q

What do curved arrows indicate in resonance structures?

A

Electron movement for pairs of electrons

Curved arrows show where electrons are moving from and to.

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16
Q

What are the five main bonding patterns in which resonance occurs?

A
  • Allylic lone pairs
  • Allylic positive charge
  • Lone pair adjacent to a positive charge
  • Pi bond between two atoms with different electronegativities
  • Conjugated pi bonds in a ring

Recognizing these patterns helps predict resonance behavior.

17
Q

What is the significance of filled octets in assessing resonance stability?

A

The most significant resonance forms have the greatest number of filled octets

Filled octets contribute to the stability of resonance contributors.

18
Q

What distinguishes localized electrons from delocalized electrons?

A

Localized electrons are NOT in resonance; delocalized electrons ARE in resonance

Delocalization increases stability in molecules.

19
Q

What type of hybridization do peptide bonds exhibit?

A

sp² hybridization

This affects the geometry and rotation around the C-N bond in polypeptides.

20
Q

How many localized lone pairs are present in a molecule with no unhybridized p orbitals?

A

0

Localized lone pairs cannot participate in resonance.