Chapter 8: Q54a (page 262)
Question: Which of the following alcohols could notbe made selectively by hydroboration–oxidation of an alkene? Explain.
Short Answer
Answer
Not possible
Chapter 8: Q54a (page 262)
Question: Which of the following alcohols could notbe made selectively by hydroboration–oxidation of an alkene? Explain.
Answer
Not possible
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Get started for freeCompound A, , was found to be an optically active alcohol. Despite its apparent unsaturation, no hydrogen was absorbed on catalytic reduction over a palladium catalyst. On treatment of A with dilute sulfuric acid, dehydration occurred and an optically inactive alkene B,, was the major product. Alkene B, on ozonolysis, gave two products. One product was identified as propanal,. Compound C, the other product, was shown to be a ketone,. How many degrees of unsaturation does A have? Write the reactions, and identify A, B, and C.
Compound A has the formula . On catalytic hydrogenation over palladium, it reacts with only 1 molar equivalent of . Compound A also reacts with ozone, followed by zinc treatment, to yield a symmetrical diketone, B.
Write the reactions.
Show the structures of alkenes that give the following products on oxidative cleavage with in acidic solution.
Compound A has the formula . It reacts rapidly with to give and a carboxylic acid, B , but reacts with only 1 molar equivalent of on catalytic hydrogenation over a palladium catalyst. On hydrogenation under conditions that reduce aromatic rings, 4 equivalents of are taken up and hydrocarbon C is produced. What are the structures of A, B, and C? Write the reactions.
Evidence that cleavage of 1,2-diols by occurs through a five membered cyclic periodate intermediate is based on kinetic data—the measurement of reaction rates. When diols A and B were prepared and the rates of their reaction withwere measured, it was found that diol A cleaved approximately 1 million times faster than diol B. Make molecular models of A and B and of potential cyclic periodate intermediates, and then explain the kinetic results
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