Advertisements
Advertisements
प्रश्न
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’.
Advertisements
उत्तर
\[\begin{array}{cc}
\phantom{...}\ce{CH3}\phantom{..............................}\ce{CH3}\phantom{..............................}\ce{CH3}\\
|\phantom{..................................}|\phantom{.................................}|\\
\ce{\underset{(A)}{\underset{(C4H8)}{\underset{2-Methylprop-1-ene}{H3C - C = CH2 + HCl}}} ->[Markovnikov][rule] H3C - C - CH3 ->[KOH (aq_.)Hydrolysis][\Delta] H3C - C - CH3}\\
\phantom{...................................}|\phantom{.................................}|\\
\phantom{.....................................}\ce{\underset{(B)}{\underset{2-Chloro-2-methylpropane}{Cl}}\phantom{...............}\ce{\underset{(C)}{\underset{(C4H10O)}{\underset{2-Hydroxy-2-methylpropane}{OH}}}}}
\end{array}\]
APPEARS IN
संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
Name the reagent used to bring about the following conversion.
Bromoethane to ethoxyethane
Name the reagent used to bring about the following conversion.
Ethyl bromide to ethyl isocyanide
Give reasons:
Haloarenes are less reactive than haloalkanes.
Convert the following:
Propene to propan-1-ol
Observe the following and answer the question given below.

Can it react by SN1 mechanism? Justify your answer.
Propane nitrile can be prepared by heating ____________
Explain aqueous alkaline hydrolysis of tert. butyl bromide.
In alkaline hydrolysis of tertiary butyl bromide, ____________.
Ethyl bromide undergoes the following reaction:
\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]
Which of the following is a WRONG statement?
How many metameric ethers are represented by the molecular formula C4H10O?
When C2H5Br is treated with excess of alc. NH3, the major product obtained is ____________.
The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.
What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?
Which among the following statements is not correct about SN2 reaction mechanism?
With which halogen the reactions, of alkanes are explosive?
The compound that reacts the fastest with sodium methoxide is ______.
Complete the following reactions giving a 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 a 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 reactions giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
Define and explain the SN1 mechanism with a suitable example.
What is the action of following on ethyl bromide?
alcoholic sodium hydroxide
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
Complete the following reaction, giving a 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.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
