Exam 1 Flashcards

1
Q

Constitutional Isomers

A

Same composition but differ in how their atoms connect

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

Resonance

A

represents the delocalization and stabilization of a charge

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

Bronsted Lowry Acid

A

Proton donor (will get negative charge)

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

Bronsted Lowry Base

A

Proton Acceptor (will get positive charge)

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

How does the Ka and acidity relate?

A

the larger the Ka the stronger the acid

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

How does the pKa and acidity relate?

A

The smaller the pKa the stronger the acid

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

What are the 3 factors that affect acid strength?

A

H-A bond strength, electronegativity, inductive effects

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

Explain how size and polarizability affect acidity?

A

As size and polarizability increase, It decreases the H-A bond strength, increasing acidity

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

Explain how electronegativity affects acidity?

A

As electronegativity increases, polarization increases, increasing the acidity

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

How does the number of electronegative atoms affect acidity?

A

As the number of electronegative atoms increase, the acidity increases

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

Inductive effect

A

electronegative atoms pulling electron density towards them, increasing partial positive charge on H

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

How does the stability of the conjugate base effect the acidity?

A

The more stable to conjugate base the more acidic the acid

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

Lewis Acids

A

accepts an electron pair

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

Lewis bases

A

Donate an electron pair

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

Electrophiles
Lewis acid or base?

A

loves electrons and negative charge
Lewis acid

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

Nucleophiles
Lewis acid or base?

A

Loves protons and positive chare
Lewis bases

17
Q

What are the two hydrocarbon sources?

A

Aliphatic- fats and oils, single bonds
Aromatic- essential oils, single and double bonds

18
Q

Alkynes, degrees, hybridization

A

At least one triple bond, 180, sp

19
Q

Alkanes, degrees, hybridization

A

Single bonds, 109.5, sp3

20
Q

Alkenes, degrees, hybridization

A

At least one double bond, 120, sp2

21
Q

Arenes

A

A ring of C-C double and single bonds

22
Q

What is a methylene group?

A

-CH2-

23
Q

Alkane with 11 carbons

A

Undecane

24
Q

Alkane with 12 carbons

A

Dodecane

25
Q

Explain how boiling point relates to the shape of a molecule

A

Boiling point increases with molecular weight because of intermolecular forces
the straighter the chain the more surface area there is the higher the boiling point

26
Q

Alkyl Halides

A

alkyl group bound to a halogen atom
Chloro, Fluoro, Iodo, Bromo

27
Q

Alcohols

A

Alkyl group bound to a hydroxyl group

28
Q

Conformation

A

shape of a molecule with respect to bond rotation, conforms to the most stable shape

29
Q

Staggered conformation
Types and angle

A

Bisects
Anti- 180
Gauche- 60

30
Q

Eclipse

A

Aligned
Eclipsed- 0

31
Q

What are the most and least stable conformations?
Why is it the least stable?

A

Most- Staggered anti
Least- Eclipse
Because of steric effect

32
Q

Steric

A

Increase in potential energy caused when atoms or groups are forced together closer than their radii allow

33
Q

What is the most stable cyclo bond angle?
What shape does cyclohexane take on to achieve this?

A

109.5
Chair

34
Q

Draw a Chair cyclohexane with equatorial and axial lines

A
35
Q

What happens during a ring inversion?

A

Axial groups become equatorial and vice versa
Up substituents are still up and down substituents are still down

36
Q

Stereoisomers

A

same connectivity but different positions in space