Q) complete the reaction
Asked by araima2001 | 22nd Jan, 2017, 08:10: PM
Answered by Vaibhav Chavan | 24th Jan, 2017, 11:50: AM
- Halogens are deactivators but ortho and para directors. Justify with suitable examples
- How do substituent groups (G) on an aromatic ring influence the course of electrophilic aromatic substitution?
- How do the activating and deactivating effects account for the orientation of entering E+referred?
- Explain that halogens are o-, p- directors, but are deactivating.
- Compare the rate of nitration under similar conditions of Ph-O-Me and Ph-S-Me. Explain
- Why is PhNO2 a suitable solvent for the Friedel-Crafts alkylation of PhBr while benzene is not?
- 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.
- How can a t-butyl substituent be used as a blocking group in aromatic electrophilic substitutions?
- Describe and account for the reaction , if any, of D2SO4 in D2O with (a) C6H5SO3H (b) C6H5OH (c) C6H6
Kindly Sign up for a personalised experience
- Ask Study Doubts
- Sample Papers
- Past Year Papers
- Textbook Solutions
Verify mobile number
Enter the OTP sent to your number