For each of the following compounds, indicate whether or not it can exist as cis–trans stereoisomers. If it can exist as the two isomers, draw both as a condensed structure.
(c)
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For each of the following compounds, indicate whether or not it can exist as cis–trans stereoisomers. If it can exist as the two isomers, draw both as a condensed structure.
(c)
The structure of vitamin A is shown in Problem 4.54. Is the double bond nearest the ring on the carbon chain cis or trans?
The vision process in animals involves the change of one double bond in retinal from its cis form to its trans form. The structures of cis and trans retinal are shown below. Label which is cis and which is trans.
Determine whether each of the following is the cis or the trans stereoisomer:
(b)
Draw the skeletal structure and give the name and omega number of the following fatty acid:
CH3CH2CH2CH2CH2HC=CHCH2HC=CHCH2CH2CH2CH2CH2CH2CH2COOH
Mark the chiral centers in the following molecules, if any, with an asterisk (*).
(a)