Advertisements
Advertisements
प्रश्न
Identify the major product formed when 2-cyclohexylchloroethane undergoes a dehydrohalogenation reaction. Name the reagent which is used to carry out the reaction.
Advertisements
उत्तर
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
संबंधित प्रश्न
Identify the product ‘D’ in the following sequence of reactions:
\[\ce{H3C - CH2 - CH2 - Cl \underset{KOH}{\overset{Alc}{->}} 'B' \overset{HBr}{->} 'C' \underset{Elther}{\overset{Na}{->}}'D'}\]
Identify ‘A’ and ‘B’ in the following reaction :
\[\ce{CH3 - CH = CH2 ->[HBr]'A' ->[alc.KOH]'B'}\]
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:
1-Bromo-1-methylcyclohexane
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.
The conversion of an alkyl halide into an alkene by alcoholic KOH is classified as ______.
An SN1 reaction at the asymmetric carbon of an enantiomerically pure chiral alkyl halide gives a product ______.
