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on Stre - DH
Solution
The strength of a nucleophile depends on how easily it can donate its lone pair of electrons (for a
neutral nucleophile like H 2 O) or how easily it can give away its negative charge (for a
negatively charged species like Cl -
) to a center of positive charge. In terms of electronegativity,
Fis a highly electronegative atom followed by O, then comes N and then C. So it is easier for C
to share its electrons followed by N then O then F. In other words the more is the basicity of a
nucleophile the more is its strength as a nucleophile. All nucleophiles are lewis bases. The
basicity reduces as we move from left to right in a period. The arrangement of elements in
decreasing order of basicity is
C>N>O>F
Hence this should be the decreasing order of strength of these atoms as a nucleophile. Likewise
if we compare the given options, the arrangement of these groups in increasing order of strength
of nucleophile is as shown
-F<-OH<-CN<-C 2 H 6
(C 2 H 6 - ethyl)

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  • 1. on Stre - DH Solution The strength of a nucleophile depends on how easily it can donate its lone pair of electrons (for a neutral nucleophile like H 2 O) or how easily it can give away its negative charge (for a negatively charged species like Cl - ) to a center of positive charge. In terms of electronegativity, Fis a highly electronegative atom followed by O, then comes N and then C. So it is easier for C to share its electrons followed by N then O then F. In other words the more is the basicity of a nucleophile the more is its strength as a nucleophile. All nucleophiles are lewis bases. The basicity reduces as we move from left to right in a period. The arrangement of elements in decreasing order of basicity is C>N>O>F Hence this should be the decreasing order of strength of these atoms as a nucleophile. Likewise if we compare the given options, the arrangement of these groups in increasing order of strength of nucleophile is as shown -F<-OH<-CN<-C 2 H 6 (C 2 H 6 - ethyl)