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Convert the following: 2-Chloropropane to propan-1-ol

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प्रश्न

Convert the following:

2-Chloropropane to propan-1-ol

एका वाक्यात उत्तर
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उत्तर

\[\begin{array}{cc}
\ce{H3C - CH - CH3 ->[Alc.KOH]\underset{Propene}{H3C - CH = CH2}->[HBr][Peroxide]\underset{1-Bromopropane}{H3C - CH2 - CH2Br}->[NaOH(aq.)]\underset{Propan-1-ol}{H3C - CH2 - CH2OH}}\\
|\phantom{...........................................................................................}\\
\ce{\underset{2-Chloropropane}{Cl}\phantom{..........................................................................................}}
\end{array}\]

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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. v. | पृष्ठ २३३

संबंधित प्रश्‍न

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

  1.    

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


Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.

\[\ce{2-Bromobutane->[Alc.KOH]A->[][Br2]B->[][NaNH2]C}\]


Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.

\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]


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 ____________


Nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene. Give reason.


Explain the factors affecting SN1 and SN2 mechanism.


Explain aqueous alkaline hydrolysis of tert. butyl bromide.


Which of the following is a primary halide?


What type of hybridisation is present in carbocation formed during the alkaline hydrolysis of 1- bromo-1- phenyl ethane?


\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]

Compounds X and Y are ____________.


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 ____________.


Identify 'B' in the following reaction.

\[\ce{2-Bromobutane ->[KOH alc.][\Delta] A ->[HI] B}\]


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?


The order of reactivity of the given haloalkanes towards nucleophiles is:


The compound that reacts the fastest with sodium methoxide is ______.


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.


Observe the following and answer the question given below:

Can react by SN1 mechanism? Justify your answer.


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 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.

\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}\\
\end{array}\]


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