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प्रश्न
Name the reagent used to bring about the following conversion.
Ethyl bromide to ethyl isocyanide
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उत्तर
| Reactant | Reagent | Product |
| Ethyl bromide | \[\ce{->[Alcohol][AgCN]}\] | Ethyl isocyanide |
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.
\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]
Name the reagent used to bring about the following conversion.
1-Chloropropane to 1-nitropropane
Distinguish between SN1 and SN2 mechanism of substitution reaction.
Convert the following:
Propene to propan-1-ol
Convert the following:
2-Chloropropane to propan-1-ol
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.
Propane nitrile can be prepared by heating ____________
The following will react faster by SN1 mechanism
The least reactive towards nucleophilic addition reactions is ____________.
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)
How many metameric ethers are represented by the molecular formula C4H10O?
Which one is most reactive towards nucleophilic addition reaction?
What type of hybridisation is present in carbocation formed during the alkaline hydrolysis of 1- bromo-1- phenyl ethane?
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 ______.
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 reactions giving a major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Observe the following and answer the question given below:
Can react by SN1 mechanism? Justify your answer.
Define and explain the SN1 mechanism with a suitable example.
What is the action of following on ethyl bromide?
alcoholic sodium hydroxide
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
Identify the substrate 'X' in the following reaction.
\[\ce{\underset{}{X + O2} ->[i) Co-naphtenate 423 K][ii) dil HClΔ] \underset{\underset{}{}}{Phenol + Acetone}}\]
Which of the following reagent is used for conversion of alkyl halide into nitrile?
