Organic Chemistry Reaction Flashcards

1
Q

Alkane Reactions ×2

A
  1. Combustion

2. Halogenation

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

Alkane Combustion

A

CO2+H2O

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

Alkane Halogenation

3 Steps

A

R + X2 ~> R-X + HX

Chain Initiation
Chain Propagation
Chain Termination

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

Alkenes Reaction ×7

A
  1. Hydrogenation
  2. Halogenatiom
  3. Hydrohalogenation
    All are Addition Reactions
  4. Catalytic Hydration
  5. Oxidation
    Still Addition
  6. Addition Polymerization
  7. Combustion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Alkene Hydrogenation

A

+ H2 ~> Alkane

Catalyst Ni Pd Pt

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

Alkene Halogenation

A

+ X2 ~> Dihaloalkane

No Catalyst

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

Alkene Halohydrogenation

A

+ HX ~> Haloalkane
No Catalyst
Makovnikovs Rule
H sticks with more H

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

Alkene Catalytic Hydration

A

+ H2O ~> Alcohol

Catalyst: Phosphoric Acid/ High Temp

H2O
H to Double Bond + OH to Hydroxyl

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

Alkene Oxidation

A

+ O from KMnO4 + H2O
~> Diol

Cr2O7 too weak
 No Reaction
H2O + O
2H 2O
2OH
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Alkene Polymerization

A

Monomer to Polymer

Topic 5.4

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

Alkene Combustion

A

CO2 H2O

A Waste to Use Alkenes as Fuel

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

Haloalkane Reaction ×1

A

Substitution

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

Haloalkane Substitution

A

RX + OH

~> Alcohol + X

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

Alcohol Reactions ×5

A
  1. Substitution
  2. Dehydration
  3. Oxidation
  4. Esterification
  5. Reaction with Reactive Metals
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Alcohol Substitution
Two Ways
Preparation of HBr

A

+ HX
~> Haloalkanes + H2O

Or

+PX3
~> Haloalkane + H3PO3
3OH +P to H3PO3

No Catalyst

Preparation:
KBr + H3PO4 ~> HBr + KH2PO4

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

Alcohol Dehydration
Two Ways
Primary Secondary Tertiary
Major Minor

A

+H2SO4 As Catalyst

+Al2O3 or Pumice stone with Heat As Catalyst

Primary: Alkene +H2O
Secondary: 2 Types of Alkenes +H2O
Tertiary: 2 Types of Alkenes +H2O

Major ~ More R groups connecting the C=C double bond C atom

17
Q

Alcohol Oxidation

Primary Secondary Tertiary

A

+ K2Cr2O7/H+

Primary: ~> Aldehyde + H2O ~> Carboxylic Acid
Secondary: ~> Ketones +H2O
Tertiary: No Reaction

Alcohol 2H + Oxidation O ~> H2O + Aldehyde

18
Q

Alcohol Esterification

A

+ Carboxylic Acid
~> Ester + H2O

Catalyst: H2SO4

19
Q

Alcohol Reaction with Metals

A

Only K, Na

2ROH + 2Metal ~> 2RO Metal + H2

20
Q

Aldehyde Reactions ×2

A
  1. Oxidation

2. Reduction

21
Q

Ketones Reactions

A
  1. Reduction

No Oxidation!!

22
Q

Aldehyde Oxidation

A

+ Cr2O7/H+
~> Carboxylic Acid

+ O, COH to COOH

23
Q

Aldehyde Reduction

A

~> Primary Alcohol

Agents: LiAlH4 or NaBH4
(Stronger) (Milder)

LiAlH4 reacts with water
NaBH4 does not

LiAlH4 stores in parrafin oil

Steps LiAlH4:

  1. LiAlH4/dry ether
  2. H+

Steps NaBH4
1. NaBH4, H2O

Notes:
H from agent compensate the lost C=C
H from H+ goes to OH

24
Q

Ketones Reduction

A

~> Secondary Alcohol

Agents: LiAlH4 or NaBH4
(Stronger) (Milder)

LiAlH4 reacts with water
NaBH4 does not

LiAlH4 stores in parrafin oil

Steps LiAlH4:

  1. LiAlH4/dry ether
  2. H+

Steps NaBH4
1. NaBH4, H2O

Notes:
H from agent compensate the lost C=C
H from H+ goes to OH