317213 \(+\mathrm{I}\) effect is shown by

317214 Decreasing - I effect of given groups is
(A) \({\rm{ - CN}}\)
(B) \(-\mathrm{NO}_{2}\)
(C) \(-\mathrm{NH}_{3}^{+}\)
(D) \(-F\)

317215 Identify lowest positive charge developed (indicated by \(\partial ,\,\,{\partial _1},\,\,{\partial _2},\,\,{\partial _3})\) due to inductive effect in following compounds.

317216 Chloroacetic acid is a stronger acid than acetic acid. This can be explained using

317217 Assertion :
Polarisation of one \(\sigma\) bond caused by the polarisation of adjacent \(\sigma\) bond is referred to as the inductive effect.
Reason :
The substituents can be classified as electron withdrawing or electron donating groups relative to hydrogen.

317213 \(+\mathrm{I}\) effect is shown by

317214 Decreasing - I effect of given groups is
(A) \({\rm{ - CN}}\)
(B) \(-\mathrm{NO}_{2}\)
(C) \(-\mathrm{NH}_{3}^{+}\)
(D) \(-F\)

317215 Identify lowest positive charge developed (indicated by \(\partial ,\,\,{\partial _1},\,\,{\partial _2},\,\,{\partial _3})\) due to inductive effect in following compounds.

317216 Chloroacetic acid is a stronger acid than acetic acid. This can be explained using

317217 Assertion :
Polarisation of one \(\sigma\) bond caused by the polarisation of adjacent \(\sigma\) bond is referred to as the inductive effect.
Reason :
The substituents can be classified as electron withdrawing or electron donating groups relative to hydrogen.

317213 \(+\mathrm{I}\) effect is shown by

317214 Decreasing - I effect of given groups is
(A) \({\rm{ - CN}}\)
(B) \(-\mathrm{NO}_{2}\)
(C) \(-\mathrm{NH}_{3}^{+}\)
(D) \(-F\)

317215 Identify lowest positive charge developed (indicated by \(\partial ,\,\,{\partial _1},\,\,{\partial _2},\,\,{\partial _3})\) due to inductive effect in following compounds.

317216 Chloroacetic acid is a stronger acid than acetic acid. This can be explained using

317217 Assertion :
Polarisation of one \(\sigma\) bond caused by the polarisation of adjacent \(\sigma\) bond is referred to as the inductive effect.
Reason :
The substituents can be classified as electron withdrawing or electron donating groups relative to hydrogen.

317213 \(+\mathrm{I}\) effect is shown by

317214 Decreasing - I effect of given groups is
(A) \({\rm{ - CN}}\)
(B) \(-\mathrm{NO}_{2}\)
(C) \(-\mathrm{NH}_{3}^{+}\)
(D) \(-F\)

317215 Identify lowest positive charge developed (indicated by \(\partial ,\,\,{\partial _1},\,\,{\partial _2},\,\,{\partial _3})\) due to inductive effect in following compounds.

317216 Chloroacetic acid is a stronger acid than acetic acid. This can be explained using

317217 Assertion :
Polarisation of one \(\sigma\) bond caused by the polarisation of adjacent \(\sigma\) bond is referred to as the inductive effect.
Reason :
The substituents can be classified as electron withdrawing or electron donating groups relative to hydrogen.

317213 \(+\mathrm{I}\) effect is shown by

317214 Decreasing - I effect of given groups is
(A) \({\rm{ - CN}}\)
(B) \(-\mathrm{NO}_{2}\)
(C) \(-\mathrm{NH}_{3}^{+}\)
(D) \(-F\)

317215 Identify lowest positive charge developed (indicated by \(\partial ,\,\,{\partial _1},\,\,{\partial _2},\,\,{\partial _3})\) due to inductive effect in following compounds.

317216 Chloroacetic acid is a stronger acid than acetic acid. This can be explained using

317217 Assertion :
Polarisation of one \(\sigma\) bond caused by the polarisation of adjacent \(\sigma\) bond is referred to as the inductive effect.
Reason :
The substituents can be classified as electron withdrawing or electron donating groups relative to hydrogen.