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प्रश्न
How the following conversion can be carried out?
2-Chloropropane to 1-propanol
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उत्तर
\[\begin{array}{cc}
\ce{CH3 - CH - CH3 ->[Alc. KOH, \Delta][Dehydrohalogenation] \underset{Propene}{CH3 - CH = CH2} ->[HBr,Peroxide] \underset{1-Bromopropane}{CH3 - CH2 - CH2 - Br} ->[KOH (aq.), \Delta][nucleophilic substitution] \underset{1-propanol}{CH3 - CH2 - CH2 - OH}}\\
|\phantom{.....................................................................................................................}\\
\ce{\underset{2-Chloropropane}{Cl}}\phantom{....................................................................................................................}
\end{array}\]
APPEARS IN
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
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
Write the structure of the major organic product in the following reaction:
\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]
How the following conversion can be carried out?
1-Bromopropane to 2-bromopropane
How the following conversion can be carried out?
2-Bromopropane to 1-bromopropane
Draw a neat, labelled energy profile diagram for SN1 reaction mechanism.
What are racemates?
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 ______.
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3 C(CI) (C2H5)CH2CH3 }\]
Which of the following alkyl halides will undergo SN1 reaction most readily?
