Advertisements
Advertisements
Question
Name the reagent used to bring about the following conversion.
Ethyl bromide to ethyl isocyanide
Advertisements
Solution
| Reactant | Reagent | Product |
| Ethyl bromide | \[\ce{->[Alcohol][AgCN]}\] | Ethyl isocyanide |
APPEARS IN
RELATED QUESTIONS
from the following pair would undergo SN2 faster from the other?
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
Give reasons:
Haloarenes are less reactive than haloalkanes.
Convert the following:
2-Chloropropane to propan-1-ol
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.

Can it react by SN1 mechanism? Justify your answer.
Propane nitrile can be prepared by heating ____________
Write the correct order of increasing ease of dehydrohalogenation.
\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]
\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]
\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]
In alkaline hydrolysis of tertiary butyl bromide, ____________.
Which of the following is a primary halide?
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)
Write the product formed when alkyl halide reacts with silver nitrite.
The major product formed when 2-bromobutane is treated with alcoholic KOH is ______.
With which halogen the reactions, of alkanes are explosive?
The compound that reacts the fastest with sodium methoxide is ______.
Complete the following reaction giving major products.
\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{.........}\\
\ce{CH3 - c - CH2 - Cl ->[Na/dry ether]}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]
Complete the following reaction giving a major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Observe the following and answer the question given below:

Comment on the bond length of C-X bond in it.
What is the action of following on ethyl bromide?
alcoholic sodium hydroxide
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
Identify the chiral molecule from the following.
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/ dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
