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Q1. Show that alcohols you would obtain by reduction of the following carbonyl compounds:
Q2. Give the structures of the major products you would obtain from reaction of phenol with the following reagents:
(a) Br2 (1 mol)
(b) Br2 (3 mol)
(c) NaOH, then CH3I
(d) Na2Cr2O7, H3O+
Q3. How would you prepare the following compounds from 2-phenylethanol?
(a) Benzoic acid
(b) Ethylbenzene
(c) 1-Bromo-2-phenylethane
(d) Phenylacetic acid (C6H5CH2CO2H)
(e) Phenylacetaldehyde (C6H5CH2CHO)
Q4. What products would you obtain from reaction of 1-methylcyclohexanol with the following reagents?
(a) HBr
(b) H2SO4
(c) CrO3
(d) Na
(e) Product of part (d), then CH3I
Q5. What product would you obtain from reaction of butan-1-ol with the following reagents?
(a) PBr3
(b) CrO3, H3O+
(c) A periodinane
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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