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प्रश्न
The conversion of an alkyl halide into an alkene by alcoholic KOH is classified as ______.
पर्याय
a substitution reaction
an addition reaction
a dehydrohalogenation reaction
a dehydration reaction
उत्तर
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.
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संबंधित प्रश्न
Identify the product ‘D’ in the following sequence of reactions:
\[\ce{H3C - CH2 - CH2 - Cl \underset{KOH}{\overset{Alc}{->}} 'B' \overset{HBr}{->} 'C' \underset{Elther}{\overset{Na}{->}}'D'}\]
State and explain Markownikoff's rule with suitable example
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2, 2, 3-Trimethyl-3-bromopentane
Write the structure of the major organic product in the following reaction:
\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]
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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.
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Identify the major product formed when 2-cyclohexylchloroethane undergoes a dehydrohalogenation reaction. Name the reagent which is used to carry out the reaction.
Elimination of bromine from 2-bromobutane results in the formation of ______.
