Chapter 17: Q44P (page 896)
Predict the site(s) of electrophilic attack on these compounds.
(a)
(b)
Short Answer
(a)
(b)
Chapter 17: Q44P (page 896)
Predict the site(s) of electrophilic attack on these compounds.
(a)
(b)
(a)
(b)
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Get started for freePredict the products formed when m-cresol (m-methylphenol) reacts with
(a) NaOH and then ethyl bromide
(b) CH3 acetyl chloride, CH3COCI
(c) bromine in CCI4 in the dark
(d) excess bromine in CCI4 in the light
(e) sodium dichromate in H2SO4
(f) two equivalents of tert-butyl chloride and AICI3
A common illicit synthesis of methamphetamine involves an interesting variation of the Birch reduction. A solution of ephedrine in alcohol is added to liquid ammonia, followed by several pieces of lithium metal. The Birch reduction usually reduces the aromatic ring, but in this case, it eliminates the hydroxy group of ephedrine to give methamphetamine. Propose a mechanism, similar to that for the Birch reduction, to explain this unusual course of the reaction
Propose a mechanism for the reaction of benzyl bromide with ethanol to give benzyl ethyl ether (shown above).
Predict the major products of the following reactions.
(a) toluene + excess CI2 (heat, pressure)
(b) benzamide ( PhCONH2 ) + Na (liquid NH3, CH3 CH2OH)
(c) o-xylene + H2 (1000 psi, 100 °C, Rh catalyst)
(d) p-xylene + Na (liquid NH3, CH3CH2OH )
(e)
What products would you expect from the following Suzuki coupling reactions?
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