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प्रश्न
Convert the following:
2-Chloropropane to propan-1-ol
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उत्तर
\[\begin{array}{cc}
\ce{H3C - CH - CH3 ->[Alc.KOH]\underset{Propene}{H3C - CH = CH2}->[HBr][Peroxide]\underset{1-Bromopropane}{H3C - CH2 - CH2Br}->[NaOH(aq.)]\underset{Propan-1-ol}{H3C - CH2 - CH2OH}}\\
|\phantom{...........................................................................................}\\
\ce{\underset{2-Chloropropane}{Cl}\phantom{..........................................................................................}}
\end{array}\]
APPEARS IN
संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
Complete the following reaction giving major products.
\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}\ce{CH3\phantom{................}}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3\phantom{................}}
\end{array}\]
Name the reagent used to bring about the following conversion.
Ethyl bromide to ethyl isocyanide
Convert the following:
Propene to propan-1-ol
Convert the following:
Benzyl alcohol to benzyl cyanide
Convert the following:
tert-Butyl bromide to isobutyl bromide
HCl is added to a hydrocarbon ‘A’ \[\ce{(C4H8)}\] to give a compound ‘B’ which on hydrolysis with aqueous alkali forms tertiary alcohol ‘C’ \[\ce{(C4H10O)}\]. Identify ‘A’ ,‘B’ and ‘C’.
Observe the following and answer the question given below.
Name the type of halogen derivative.
Observe the following and answer the question given below.
Comment on the bond length of C–X bond in it.
Observe the following and answer the question given below.
Can it react by SN1 mechanism? Justify your answer.
Nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene. Give reason.
Write the correct order of increasing ease of dehydrohalogenation.
\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]
\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]
\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]
The least reactive towards nucleophilic addition reactions is ____________.
Which of the following is least reactive towards nucleophilic addition?
The following mechanism has been proposed for the reaction of NO2 with F2 to form NO2F:
\[\ce{NO2_{(g)} + F2_{(g)} -> NO2F_{(g)} + F_{(g)} (slow)}\]
\[\ce{F_{(g)} + NO2_{(g)} -> NO2F_{(g)} (fast)}\]
The order of the reaction with respect to NO2(g)
The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.
Identify major product 'B' in the following reaction.
\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
Explain the dehydrohalogenation reaction of 2-chlorobutane.
Complete the following reaction sequences by writing the structural formulae of the organic compounds 'A', 'B' and 'C'.
\[\ce{2-Bromobutan ->[alc. KOH] A ->[][Br2] B ->[][NANH2] C}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/ dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
Which of the following pair of compounds on heating gives butanenitrile?
Which of the following reagent is used for conversion of alkyl halide into nitrile?
