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Question
Complete the reaction with the main product formed:

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Solution

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RELATED QUESTIONS
How the following conversion can be carried out?
Ethyl chloride to propanoic acid.
Given reasons: SN1 reactions are accompanied by racemization in optically active alkyl halides.
Which of the following is a primary halide?
SN2 mechanism proceeds through intervention of ____________.
Identify X and Y in the following sequence:
\[\ce{C2H5Br ->[X] Product ->[Y] C3H7NH2}\]
Which of the following compound will undergo racemisation when reacts with aq. KOH?
(i)

(ii)
CH3CH2CH2Cl
(iii)
\[\begin{array}{cc}
\ce{CH3}\phantom{..}\\
|\phantom{....}\\
\ce{CH3-CH-CH2Cl}
\end{array}\]
(iv)
\[\begin{array}{cc}
\phantom{..}\ce{H}\\
\phantom{..}|\\
\ce{CH3-C-Cl}\\
\phantom{..}|\\
\phantom{.....}\ce{C2H5}
\end{array}\]
Which of the following statements are correct about this reaction?

(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
Racemisation occurs in ______.
Convert bromoethane to propanamine.
Give the mechanism of the following reaction:
\[\ce{CH3CH2OH ->[H2SO4][413 K] CH3CH2-O-CH2CH3 + H2O}\]
