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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
\[\begin{array}{cc}
\phantom{...........................................}\ce{CH3}\\
\phantom{.......................................}|\\
\ce{\underset{tert-Butyl bromide}{(CH3)3CBr} + KOH->[ethanol, \Delta][Dehydrohalogenation] \underset{2-methylpropene}{CH3 - C = CH2} + KBr + H2O}\
\end{array}\]
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
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?
2-Chloropropane to 1-propanol
How the following conversion can be carried out?
2-Bromopropane to 1-bromopropane
'A' is:
Deamination of meso- di bromobutane gives mainly:-
Elimination of bromine from 2-bromobutane results in the formation of ______.
A primary alkyl halide would prefer to undergo ______.
Reaction of trans-2-phenyl-1-bromocyclopentane with alcoholic KOH produces.
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 ______.
