do i and iii both retro and forward rxn in detail (b) Visualise the retrosynthesis for thetargetcompounds(asfollowinginstructed) along with synthesis:(2)(ti)(iii)(Naphthalene has to be one of용PhOH OHthe equivalent reagents)(1,3-di X disconnection hasto be followed)

Answered: Image /qna-images/answer/f6135286-787d-4b97-ab0b-03618f426ba4.jpg

(b) Visualise the retrosynthesis for the (as following instructed) (i) (ti) PH target compounds along with synthesis: (Naphthalene has to be one of the equivalent reagents) OH OH (1,3-di X disconnection has to be followed)

(b) Visualise the retrosynthesis for the (as following instructed) (i) (ti) PH target compounds along with synthesis: (Naphthalene has to be one of the equivalent reagents) OH OH (1,3-di X disconnection has to be followed)

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 45MP

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Question

do i and iii both retro and forward rxn in detail

(b) Visualise the retrosynthesis for the
target
compounds
(as
following
instructed) along with synthesis:
(2)
(ti)
(iii)
(Naphthalene has to be one of
용
Ph
OH OH
the equivalent reagents)
(1,3-di X disconnection has
to be followed)

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