Lesson 12 of 15 • 1 upvotes • 13:03mins

Carboxylic acids that have a carbonyl group two carbons over (this is called the “beta” position) can lose carbon dioxide quite readily – heating above 150 degrees C will do the trick.
15 lessons • 3h 1m
1.1 Brief Introduction Of Myself (in Hindi)
2:02mins
1.2 Overview (in Hindi)
10:55mins
2.0 Introduction To Carboxylic Acids (in Hindi)
11:27mins
3.1 Preparation Of Carboxylic Acids : From Hydrocarbons (in Hindi)
11:15mins
3.2 Preparation Of Carboxylic Acids : From Cyanides (in Hindi)
11:59mins
3.3 Preparation Of Carboxylic Acids : From Grignard Reagent (in Hindi)
9:11mins
4.0 Acidic Strength Of Carboxylic Acids (in Hindi)
14:11mins
Preparation Of Acid Chlorides : From Carboxylic Acids (in Hindi)
14:04mins
Formation Of Acid Anhydrides : From Carboxylic Acids (in Hindi)
14:23mins
Preparation Of Acid Amides : From Carboxylic Acids (in Hindi)
14:46mins
Part 1. Decarboxylation Of Acids : Soda lime Process (in Hindi)
12:48mins
Part 2. Decarboxylation Of Acids : Heating Effect On Beta-keto Acids (in Hindi)
13:03mins
Part 3. Decarboxylation Of Acids : Heating Effect On Geminal Dicarboxylic acids (in Hindi)
12:20mins
Part1. Kolbey's Electrolysis : Preparation Of Alkanes (in Hindi)
14:04mins
Part2. Kolbey's Electrolysis : Preparation Of Alkanes (in Hindi)
15:00mins