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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

How do polar solvents help in the first step in SN1 mechanism?

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प्रश्न

How do polar solvents help in the first step in SN1 mechanism?

टीपा लिहा
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उत्तर

The SN1 mechanism proceeds through the formation of carbocation. It involves breaking of C-halogen bond for which energy is obtained through the salvation of halide ion with the proton of the protic solvent. Thus, polar solvents help in ionisations step by stabilizing the ions by solvation.

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पाठ 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ १४४]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 10 Haloalkanes and Haloarenes
Exercises | Q III. 67. | पृष्ठ १४४

संबंधित प्रश्‍न

Which would undergo SN1 reaction faster in the following pair and why?


Given reasons: C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.


Write the isomers of the compound having the formula C4H9Br.


What is the action of the following on ethyl bromide:
moist silver oxide


Answer the following question.
Write one stereochemical difference between SN1 and SN2 reactions.


Which of the following reactions is an example of nucleophilic substitution reaction?


Which one is most reactive towards SN1 reaction?


Which of the following compounds is optically active?


The increasing order of nucleophilicity would be:


Which of the following compound will undergo racemisation when reacts with aq. KOH?

(i)

(ii)

CH3CH2CH2Cl

(iii)

\[\begin{array}{cc}
\ce{CH3}\phantom{..}\\
|\phantom{....}\\
\ce{CH3-CH-CH2Cl}
\end{array}\]

(iv)

\[\begin{array}{cc}
\phantom{..}\ce{H}\\
\phantom{..}|\\
\ce{CH3-C-Cl}\\
\phantom{..}|\\
\phantom{.....}\ce{C2H5}
\end{array}\]


The increasing order of reactivity towards SN1 mechanism is:

(I) \[\begin{array}{cc}
\ce{CH3-CH-CH2-CH3}\\
|\phantom{........}\\
\ce{CH3}\phantom{.....}
\end{array}\]

(II) CH3CH2CH2Cl

(III) P–CH3O–C6H4–CH2Cl


Which of the following compounds will give a racemic mixture on nucleophilic substitution by OH ion?

1-Bromoethane, 1-Bromopropane, 1-Bromobutane, Bromobenzene


A primary alkyl halide would prefer to undergo ______.


Which of the compounds will react faster in SN1 reaction with the –OH ion?

\[\ce{CH3-CH2-Cl}\] or \[\ce{C6H5-CH2-Cl}\]


Which of the following is the definition of chirality?


Give reason for the following:

The product formed during SN1 reaction is a racemic mixture.


 Acetic anhydride from acetic acid


The compound that will undergo SN1 reaction with the fastest rate is:


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