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CBSE Class 11-science Answered

Hydrocarbons
Asked by guptaserendri | 01 Jul, 2020, 03:58: PM
Expert Answer
Answered by Ramandeep | 10 Jul, 2020, 03:52: PM
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CBSE 11-science - Chemistry
Ch3 ch2 cl
Asked by maibamjohnny89 | 15 Jan, 2022, 09:38: PM
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CBSE 11-science - Chemistry
Halogens are deactivators but ortho and para directors. Justify with suitable examples
Asked by dubeyanubhav65 | 18 Jan, 2021, 09:52: PM
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CBSE 11-science - Chemistry
Hydrocarbons
Asked by guptaserendri | 01 Jul, 2020, 03:58: PM
ANSWERED BY EXPERT
CBSE 11-science - Chemistry
How do substituent groups (G) on an aromatic ring influence the course of electrophilic aromatic substitution?
Asked by Topperlearning User | 24 Jul, 2014, 03:46: PM
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CBSE 11-science - Chemistry
How do the activating and deactivating effects account for the orientation of entering E+referred?
Asked by Topperlearning User | 25 Jul, 2014, 07:11: AM
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CBSE 11-science - Chemistry
Explain that halogens are o-, p- directors, but are deactivating.
Asked by Topperlearning User | 01 Jun, 2016, 02:59: PM
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CBSE 11-science - Chemistry
Compare the rate of nitration under similar conditions of Ph-O-Me and Ph-S-Me. Explain
Asked by Topperlearning User | 01 Jun, 2016, 02:54: PM
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CBSE 11-science - Chemistry
Why is PhNO2 a suitable solvent for the Friedel-Crafts alkylation of PhBr while benzene is not?
Asked by Topperlearning User | 04 Jun, 2014, 01:23: PM
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CBSE 11-science - Chemistry
Account for the greater reactivity and the o, p-orientation in electrophilic substitution of biphenyl despite the electron-attracting inductive effect of the phenyl group.
Asked by Topperlearning User | 25 Jul, 2014, 07:18: AM
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CBSE 11-science - Chemistry
How can a t-butyl substituent be used as a blocking group in aromatic electrophilic substitutions?
Asked by Topperlearning User | 01 Jun, 2016, 02:54: PM
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