Chapter 14: Q 14-14-60 E (page 447)
Adiponitrile, a starting material used in the manufacture of nylon, can be prepared in three steps from 1,3-butadiene. How would you carry out this synthesis?
Short Answer
The first step of the three is-
Chapter 14: Q 14-14-60 E (page 447)
Adiponitrile, a starting material used in the manufacture of nylon, can be prepared in three steps from 1,3-butadiene. How would you carry out this synthesis?
The first step of the three is-
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Get started for freeDi-tert-butyl-1,3-butadiene does not undergo Diels-Alder reactions. Explain.
Luminol, which is used by forensic scientists to find blood, fluoresces as a result of Diels-Alder like process. The dianion of luminal reacts with to form an unstable peroxide intermediate that then loses nitrogen to form a dicarboxylate and emit light. The process is similar to that in 14-21 and 14-22. Propose a mechanism for this process.
Give IUPAC names for the following compounds:
Hydrocarbon A, C10H14, has a UV absorption at and gives hydrocarbon B, C10H18, on catalytic hydrogenation. Ozonolysis of A, followed by zinc/acetic acid treatment, yields the following di-keto dialdehyde:
c)Write the reactions, showing the starting material and products.
Which of the following dienes have an s-cis conformation, and which have an s-trans conformation? Of the s-trans dienes, which can readily rotate to s-cis?
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