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प्रश्न
Answer the following question.
Write one stereochemical difference between SN1 and SN2 reactions.
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उत्तर
SN1 reactions lead to the formation of racemic mixture whereas SN2 reactions lead to inversion in the configuration of a product.
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संबंधित प्रश्न
Write the structure of an isomer of compound C4H9Br which is most reactive towards SN1 reaction
Write the isomers of the compound having the formula C4H9Br.
Which compound in the following pair will react faster in SN2 reaction with OH−?
CH3Br or CH3I
What is the action of the following on ethyl bromide?
silver acetate
Most reactive halide towards SN1 reaction is ____________.
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
Assertion: KCN reacts with methyl chloride to give methyl isocyanide.
Reason: CN– is an ambident nucleophile.
CCl4 is insoluble in water because:-
Give reason for the following:
The product formed during SN1 reaction is a racemic mixture.
Optical activity of an enantiomeric mixture is +12.6° and the specific rotation of (+) isomer is +30°. The optical purity is ______ %.
