please help solve all. i keep gettting them wrong Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms.a = acceptord = donorn = no effect1.-S-CH33.methanesulfonyl:0:2. -P-OCH₂CH3 Inductive effectOCH₂CH3Inductive effect:0:C—CH,CH,CH,N(CH3)2. Resonance effectResonance effectInductive effectResonance effect The following reaction scheme shows the conditions for the formation of dinitro methyl benzoate, compound B, via compound A.obCH3OHNO3, H₂SO4a Draw the structure of compound A.AHNO3, H₂SO4B• Remember to include all of the formal charges on the atoms of any nitro groups.

A) The group that that donate electron to a conjugated system due to resonance is called electron…

Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms. a = acceptor d = donor n = no effect 1. 2. 3. :0: Ö: 0: methanesulfonyl -CH3 :0: -OCH₂CH3 OCH₂CH3 Inductive effect Inductive effect —C—CH,CH,CH,N(CH3)2 Resonance effect Resonance effect Inductive effect Resonance effect

Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms. a = acceptor d = donor n = no effect 1. 2. 3. :0: Ö: 0: methanesulfonyl -CH3 :0: -OCH₂CH3 OCH₂CH3 Inductive effect Inductive effect —C—CH,CH,CH,N(CH3)2 Resonance effect Resonance effect Inductive effect Resonance effect

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

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please help solve all. i keep gettting them wrong

Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms.
a = acceptor
d = donor
n = no effect
1.
-S-CH3
3.
methanesulfonyl
:0:
2. -P-OCH₂CH3 Inductive effect
OCH₂CH3
Inductive effect
:0:
C—CH,CH,CH,N(CH3)2
. Resonance effect
Resonance effect
Inductive effect
Resonance effect

The following reaction scheme shows the conditions for the formation of dinitro methyl benzoate, compound B, via compound A.
ob
CH3
O
HNO3, H₂SO4
a Draw the structure of compound A.
A
HNO3, H₂SO4
B
• Remember to include all of the formal charges on the atoms of any nitro groups.

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