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Convert the following: Ethanol to propane nitrile

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प्रश्न

Convert the following:

Ethanol to propane nitrile

रासायनिक समीकरणे/रचना
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उत्तर

\[\ce{\underset{Ethanol}{CH3CH2OH} + HCl ->[Groove's][process]\underset{Chloroethane}{CH3CH2Cl} ->[Alc.KCN,\Delta][-H2O] \underset{Propane nitrile}{CH3CH2CN}}\]

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पाठ 10: Halogen Derivatives - Exercises [पृष्ठ २३३]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
पाठ 10 Halogen Derivatives
Exercises | Q 6. iii. | पृष्ठ २३३

संबंधित प्रश्‍न

from the following pair would undergo SN2 faster from the other?

  1.    

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.

Bromoethane to ethoxyethane


Arrange the following in the increasing order of boiling points.

  1. 1-Bromopropane
  2. 2- Bromopropane
  3. 1- Bromobutane
  4. 1-Bromo-2-methylpropane

Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

Propene to propan-1-ol


Convert the following:

Benzyl alcohol to benzyl cyanide


Convert the following:

2-Chloropropane to propan-1-ol


Observe the following and answer the question given below.

Name the type of halogen derivative.


Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.


Explain the factors affecting SN1 and SN2 mechanism.


What is dehydrohalogenation? State the rule for the formation of the preferred product of dehydrohalogenation.


The least reactive towards nucleophilic addition reactions is ____________.


Which of the following is least reactive towards SN1 reactions?


Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.


Which one is most reactive towards nucleophilic addition reaction?


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 ____________.


With which halogen the reactions, of alkanes are explosive?


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 questions 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.


Discuss β - elimination reaction.


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 among the following is NOT benzylic halide?


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