Advertisements
Advertisements
Question
The conversion of an alkyl halide into an alkene by alcoholic KOH is classified as ______.
Options
a substitution reaction
an addition reaction
a dehydrohalogenation reaction
a dehydration reaction
Advertisements
Solution
The conversion of an alkyl halide into an alkene by alcoholic KOH is classified as a dehydrohalogenation reaction.
Explanation:
When an alkyl halide is treated with an alcoholic solution of potassium hydroxide (KOH), hydrogen halide is removed. It leads to the production of alkene. This is an example of a dehydrohalogenation (β-elimination) reaction.
APPEARS IN
RELATED QUESTIONS
Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:
1-Bromo-1-methylcyclohexane
Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:
2, 2, 3-Trimethyl-3-bromopentane
Write the structure of the major organic product in the following reaction:
\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]
How the following conversion can be carried out?
2-Chloropropane to 1-propanol
What are racemates?
Observe the following compounds and answer the questions given below.

(I)
\[\ce{\underset{\text{(II)}}{CH3 - CH2 - Br}}\]
- Identify the type of halides.
- Explain the nature of the C – Br bond in both of these halides.
- Which of these compounds will undergo aqueous alkaline hydrolysis readily? Write the reaction in support of your answer.

'A' is:
Identify the major product formed when 2-cyclohexylchloroethane undergoes a dehydrohalogenation reaction. Name the reagent which is used to carry out the reaction.
A primary alkyl halide would prefer to undergo ______.
Major products A and B formed in the following reaction sequence are:

