Advertisements
Advertisements
Question
Identify the major product formed when 2-cyclohexylchloroethane undergoes a dehydrohalogenation reaction. Name the reagent which is used to carry out the reaction.
Solution
The major product formed when 2-cyclohexylchloroethane undergoes dehydrohalogenation reaction is 1- cyclohexylethene. The reagent which is used to carry out the reaction is ethanolic KOH.
APPEARS IN
RELATED QUESTIONS
State and explain Markownikoff's rule with suitable example
How do you convert: 2-bromobutane to but-2-ene
Write the main products when n-butyl chloride is treated with alcoholic KOH.
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:
\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]
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:
Deamination of meso- di bromobutane gives mainly:-
Elimination of bromine from 2-bromobutane results in the formation of ______.
