Aliphatic Organic Flashcards

(39 cards)

1
Q

Acyl chloride > 2 Amide

A

RNH2, reflux, RTP (Acylation)

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

Acyl chloride > Ester

A

1 Alcohol, RTP (Acylation)

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

Amide > Carboxylic acid

A

Dilute HCl (Acid hydrolysis)

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

Acyl chloride > 1 Amide

A

concentration NH3, RTP (Acylation)

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

Acyl chloride > Carboxylic acid

A

Water, RTP (Acylation)

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

Carboxylic acid > Acyl chloride

A

SOCl2, RTP

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

Ester > Carboxylic acid

A

H+ catalyst, RTP

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

Carboxylic acid > Ester

A

1 Alcohol, H+ catalyst, RTP (Esterification)

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

Ester > 1 Alcohol

A

H+ catalyst, RTP

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

1 Alcohol > Ester

A

Carboxylic acid, H+ catalyst (Esterification)

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

Carboxylic acid > Aldehyde

A

LiAlH4, dry ether (Reduction)

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

Aldehyde > Hydroxynitrile

A

H2SO4, KCN/HCN, RTP (N.A.)

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

Aldehyde > Carboxylic acid

A

K2Cr2O7, H+ catalyst, reflux (oxidation)

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

1 Alcohol > Aldehyde

A

K2Cr2O7, H+ catalyst, distillation (oxidation)

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

Nitrile > Carboxylic acid

A

H2SO4, reflux (Acid hydrolysis)

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

Haloalkane > Grignard

A

Mg, dry ether, reflux

17
Q

Grignard > Carboxylic acid

18
Q

Haloalkane > 1 Amine

A

conc NH3, ethanol, high pressure (N.S.)

19
Q

Nitrile > 1 Amine

A

H2, Pt catalyst (Reduction)

20
Q

Haloalkane > 1 Alcohol

21
Q

Haloalkane > Nitrile

A

KCN/HCN, ethanol (N.S.)

22
Q

1 Alcohol > Alkene

A

Excess H2SO4, heat (Elimination)

23
Q

1 Alcohol > Haloalkane

A

HX, H2SO4 catalyst

24
Q

Alkene > 1 Alcohol

A

H3PO4, steam, 300C

25
Ketone > 2 Alcohol
LiAlH4, dry ether (Reduction)
26
2 Alcohol > Ketone
K2Cr2O7, H+ catalyst, reflux (oxidation)
27
Ketone > Hydroxynitrile
H2SO4, KCN/HCN, RTP (N.A.)
28
Alkylhydrogensulfate > 2 Alcohol
H2O
29
Haloalkane > 2 Alcohol
NaOH, reflux (N.S.)
30
Alkene > Haloalkane
HX (E.A.)
31
Alkene > Alkylhydrogensulfate
H2SO4, RTP
32
Alkene > Dihaloalkane
X2 (E.A)
33
Alkene > Diol
KMNO4, H2O
34
Alkene > Alkane
H2, Ni catalyst, heat
35
Alkane > Alkene
Cracking, heat
36
Alkane > Haloalkane
HX, UV (Free radical substitution)
37
Alkene > Polyalkene
High pressure
38
Free radical substitution
Initiation: Cl2 > 2Cl* Propagation 1: Cl* + C4H10 > C4H9* + HCl C4H9* + Cl2 > C4H9Cl + Cl* Termination: 2Cl* > Cl2 2C4H9* > C8H18 Cl* + C4H9* > C4H9Cl
39
Haloalkane > Alkene
NaOH Elimination