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Mithoron
Mithoron
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When Reaction of 1,3 dimethy 2-dimethyl-2,5 Dintrobenzene is the substrate what would happen if-dintrobenzene with NaOMe/MeOH is given to this compound?

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I have looked through articles and closest I feel is in this question there will be a nucleophilic aromatic substitution. Now A, a lot of questions are available where Therethere is a halogen and OMe group substitutes the halogen.

My take on this is maybe due to SIR effect (Stericsteric inhibition of resonance) The NO2 group present in between the two Methylmethyl groups would be substituted by OMe? Will this be the approach?

When 1,3 dimethy 2,5 Dintrobenzene is the substrate what would happen if NaOMe/MeOH is given to this compound?

enter image description hereI have looked through articles and closest I feel is in this question there will be a nucleophilic aromatic substitution. Now A lot of questions are available where There is a halogen and OMe group substitutes the halogen.

My take on this is maybe due to SIR effect (Steric inhibition of resonance) The NO2 group present in between the two Methyl groups would be substituted by OMe? Will this be the approach?

Reaction of 1,3-dimethyl-2,5-dintrobenzene with NaOMe/MeOH

enter image description here

I have looked through articles and closest I feel is in this question there will be a nucleophilic aromatic substitution. Now, a lot of questions are available where there is a halogen and OMe group substitutes the halogen.

My take on this is maybe due to SIR effect (steric inhibition of resonance) The NO2 group present in between the two methyl groups would be substituted by OMe? Will this be the approach?

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Daivik
Daivik
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When 1,3 dimethy 2,5 Dintrobenzene is the substrate what would happen if NaOMe/MeOH is given to this compound?

enter image description hereI have looked through articles and closest I feel is in this question there will be a nucleophilic aromatic substitution. Now A lot of questions are available where There is a halogen and OMe group substitutes the halogen.

My take on this is maybe due to SIR effect (Steric inhibition of resonance) The NO2 group present in between the two Methyl groups would be substituted by OMe? Will this be the approach?