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From the following pair would undergo SN2 faster from the other? a. b. - Chemistry

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प्रश्न

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

a.     b.

एका वाक्यात उत्तर

उत्तर

Compound (a) will undergo SN2 mechanism faster than (b).

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पाठ 10: Halogen Derivatives - Exercises [पृष्ठ २३२]

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बालभारती Chemistry [English] 12 Standard HSC
पाठ 10 Halogen Derivatives
Exercises | Q 2. iv. a. | पृष्ठ २३२

संबंधित प्रश्‍न

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

a. CH3CH2CH2I      b. CH3CH2CH2Cl


Name the reagent used to bring about the following conversion.

1-Chloropropane to 1-nitropropane


Name the reagent used to bring about the following conversion.

Chlorobenzene to biphenyl


Distinguish between SN1 and SN2 mechanism of substitution reaction.


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.

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.


Major product of the following reaction is _______________

\[\ce{CH3-CH2-Mg-Br + NH3 ->?}\]


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


Write the correct order of increasing ease of dehydrohalogenation.

\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]

\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]

\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]


Explain the factors affecting SN1 and SN2 mechanism.


Which of the following is a primary halide?


Ethyl bromide undergoes the following reaction:

\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]

Which of the following is a WRONG statement?


Which of the following is least reactive towards nucleophilic addition?


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


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


Identify major product 'B' in the following reaction.

\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]


What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?


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


Explain the dehydrohalogenation reaction of 2-chlorobutane.


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 reactions giving major product.

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


What is the action of following on ethyl bromide?

alcoholic sodium hydroxide


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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