Arrange the following alkyl halides in decreasing order of the rate of β-elimination reaction with alcoholic KOH.

A. 

B. CH3-CH2-Br

C. CH3-CH2-CH2-Br

1. A>B>C

2. C>B>A

3. B>C>A

4. A>C>B

Hint: Stability of alkene decide the rate of reaction

Alkyl halides on heating with alcoholic potash elminates one molecule of HX to form an alkene. Hydrogen is eliminated from β-carbon atom, thus this reaction is know as β-elimination reaction. Stability of product that is alkene determines rate of reaction.
 
The 3° alkyl halide will give more subtituted alkene and it is most stable alkene. The 1° alkyl halide give less substituted alkene has it is least reactive. The order is as follows:
 
i.e., 3°>2°>1° or A>C>B