Download presentation
Presentation is loading. Please wait.
Published byMelvin Harris Modified over 9 years ago
1
Dehydration of Alcohols
2
C - C X Y To make C=C need to eliminate X, Y. Elimination Reactions
3
C - C X Y 1. Concerted (x and y leave same time) 2. X leaves first 3. Y leaves first 3 ways to break 2 bonds
4
Leaving Group
5
Base Removes Proton
6
Animation
7
R-XR + + X - Alkene + H + E1 Reaction
8
Elimination 1 bond at a time E1
9
Substitution Elimination Rearrangement SN1SN1 E1 R+R+
10
SN1SN1
11
C - C X H Strong base Dehydrohalogenation
12
C-D bond stronger than C-H bond. Mechanism of Dehydrohalogenation
13
NaOEt k H /k D = 7 Isotope Effect
14
Isotope effect shows that C-H bond broken in the transition state. Isotope Effect
15
Change Element I > Br > Cl Element Effect
16
Same Side Opposite Side SYN vs. ANTI Elimination
17
Example
18
Animation
19
Product Starting Material Energy Transition State
20
Elimination 2 Bonds at a time E2
21
Procedure
22
1.Put cyclohexanol and sulfuric acid in round bottom flask 1.Fractional Distillation (steam distillation) collect distillate 80-85 o 3.Dry product with K 2 CO 3 4. Distill Procedure
23
P T = P A + P B (Steam Distillation) Distil immiscible liquids
24
Potassium Permanganate KMnO 4 Baeyer Unsaturation Tests
26
Addition of Bromine
27
Bromine and Cyclohexene
28
Animation
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.