а. Cl2, FeCl3 OMe H. b. HN HNO3 H2SO4 OMe С. NaOD D20 'Br

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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question

Finish the organic synthesis reaction

а.
Cl2,
FeCl3
OMe
H.
b.
HN
HNO3
H2SO4
OMe
С.
NaOD
D20
'Br
Transcribed Image Text:а. Cl2, FeCl3 OMe H. b. HN HNO3 H2SO4 OMe С. NaOD D20 'Br
d.
1. HCI, NaNO2
(еxcess)
ОН
H2, Pd/C
2. KI
`NH2
(ехсess)
NO2
е.
HO
HO.
Br2
note: catalyst
not necessary
on this ring!
OMe
Transcribed Image Text:d. 1. HCI, NaNO2 (еxcess) ОН H2, Pd/C 2. KI `NH2 (ехсess) NO2 е. HO HO. Br2 note: catalyst not necessary on this ring! OMe
Expert Solution
Step 1

The position of substitutions at benzene ring takes place on the basis of substituents aatached on it.

It may be ortho, para direction groups also known as ring activating groups, these are electron releasing groups.

It may be meta directing groups also known as ring deactivating groups, these are electron withdrawing groups.

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