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प्रश्न
Write the structure of the major organic product in the following reaction:
\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]
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उत्तर
\[\begin{array}{cc}
\phantom{...........................................}\ce{CH3}\\
\phantom{.......................................}|\\
\ce{\underset{tert-Butyl bromide}{(CH3)3CBr} + KOH->[ethanol, \Delta][Dehydrohalogenation] \underset{2-methylpropene}{CH3 - C = CH2} + KBr + H2O}\
\end{array}\]
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संबंधित प्रश्न
Identify ‘A’ and ‘B’ in the following reaction :
\[\ce{CH3 - CH = CH2 ->[HBr]'A' ->[alc.KOH]'B'}\]
State and explain Markownikoff's rule with suitable example
How do you convert 2-bromobutane to but-2-ene?
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-Chloro-2-methylbutane
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
How will you bring about the following conversion?
But-1-ene to but-2-ene
How the following conversion can be carried out?
1-Bromopropane to 2-bromopropane
How the following conversion can be carried out?
2-Chloropropane to 1-propanol
Draw a neat, labelled energy profile diagram for SN1 reaction mechanism.
Deamination of meso- di bromobutane gives mainly:-
Elimination of bromine from 2-bromobutane results in the formation of ______.
The conversion of an alkyl halide into an alkene by alcoholic KOH is classified as ______.
A primary alkyl halide would prefer to undergo ______.
Which of the following alkyl halides will undergo SN1 reaction most readily?
An SN1 reaction at the asymmetric carbon of an enantiomerically pure chiral alkyl halide gives a product ______.
Major products A and B formed in the following reaction sequence are:
