11 Alkenes Flashcards

1
Q

Classification of Carbocations

Carbocation = Ion with a +ve-charged C

A

1° Carbocation - 0 Alkyl Group(s)
2° Carbocation - 1 Alkyl Group(s)
3° Carbocation - 2 Alkyl Group(s)
4° Carbocation - 3 Alkyl Group(s)

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

Preparation of Alkenes

Dehydrohalogenation of Halogenalkanes

A

Mechanism: Elimination

Reagent(s): Ethanolic KOH
Condition(s): Heat under reflux

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

Preparation of Alkenes

Dehydration of Alcohols

A

Mechanism: Elimination

Reagent(s): Excess concentrated H2SO4/ Al2O3/ H3PO4

Condition(s): Heat

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

Saytzeff’s Rule

A

For elimination reactions of alcohols or halogenalkanes to alkenes, the preferred product is the alkene with the greater number of alkyl groups attached to the doubly bonded carbon.

AKA

For elimination reactions of alcohols or halogenalkanes to alkenes, the preferred product is the more substituted alkene.

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

Reaction of Alkenes

Addition of Hydrogen Halides, HX

A

Reagent(s) & Condition(s): dry HX(g)

Product(s): Monosubstituted Alkane

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

Markovnikov’s Rule

A

In the addition of a Hydrogen Halide, HX to the C=C bond of an unsymmetrical Alkene, the major product is the one in which the H atom of HX attaches itself to the doubly bonded carbon atom already bonded with the greater number of H atoms.

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

Mechanism-based Markovnikov’s Rule

A

In an Electrophile Addition reaction, the Electrophile adds to the unsymmetrical Alkene to produce the more stable Carbocation intermediate. Being formed faster in the slow step, the more stable Carbocation is more available to participate in the fast step to give the major product.

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

Reaction of Alkenes

Addition of Water, H2O (Laboratory Method)

A

Step 1
Reagent(s) & Condition(s): cold, concentrated H2SO4

Step 2
Reagent(s) & Condition(s): H2O, Heat

Product(s): Alcohol

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

Reaction of Alkenes

Addition of Steam, H2O(g) (Industrial Method)

A

Reagent(s) & Condition(s): H3PO4 on silica, high temperature and pressure

Product(s): Alcohol

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

Reactions of Alkenes

Addition of Halogens, X2 in CCl2

A

Reagent(s) & Condition(s): X2 in CCl4

Product(s): Disubstituted Alkane

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

Reactions of Alkenes

Addition of Halogens, X2 in H2O

A

Reagent(s) & Condition(s): X2 in H2O

Product(s): Monochlorinated Alcohol and Hydrogen Halide

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

Reactions of Alkenes

Mild Oxidation in Cold, Alkaline Medium

A

Reagent(s) & Condition(s): KMnO4 (aq), NaOH (aq), Cold

Product(s): Diol

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

Reactions of Alkenes

Strong Oxidation in Hot, Acidic Medium

A

Reagent(s) & Condition(s): KMnO4, H2SO4, Heat

Product(s): Carboxylic Acids, Ketones or Carbonic Acid/ Ethandioic Acid–> CO2 & H2O

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

Reactions of Alkenes

Addition of Hydrogen, H2

A

Reagent(s) & Condition(s) 1: H2, Ni & Heat
Reagent(s) & Condition(s) 2: H2, Palladium, Pd
Reagent(s) & Condition(s) 3: H2, Platinum, Pt

Product(s): Alkanes

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