Aliphatic Hydrocarbons

Multiple choice questions: 1. The catalytic hydrogenation is more easier is case of which alkenes: (a) (b) (c) (d)

2. The compound most likely to decolourize a solution of potassium permanganate is:

(a) CH3 CH 2CH3

(b)

CH3CH3

(c)

CH3CH = CHCH2CH3

(d)

3. Quinoline is used for preparation of (a) Baeyer Reagent (b) Lindlar catalyst (c) Raney Nickel (d) Divinyl Acetylene

4. Oxalic acid is prepared by ______in the presence of KMnO4 (a) Oxidation of Alkenes (b) Oxidaton of Alkanes (c) Substitution of Alkanes (d) All

5. Electrophile can attack easily to ________ (a) Alkanes (b) Alkynes (c) Alkenes (d) Benzene

6. Organic solvent used in polymerization for preparation of Rubber is (a) Benzene Short Questions: 1. Industrial preparation of Slaked lime and Ethyne. (b) Neoprene (c) Acetone (d) None of these

2. Production of Formaldehyde from Oxidation reactions of Alkenes. 3. For preparation of Alkenes, why we prefer partial hydrogenation of alkynes rather than complete hydrogenation? 4. Structural formula for Buta-1,3-diene and 3-Methyl-1 pentene-4-yne. 5. Write down two tests used for detection of unsaturation. Extensive Questions: Explain Acidic Nature of Alkynes with Internal Alkynes, Also explains which alkynes are more acidic? 04 Explain Kolbs Electrolytic method for preparation of Alkynes? Reactions of Alkenes with halogen acids 05 05