Chapter 10: Q.8. (page 390)
Question: Draw the structure corresponding to each IUPAC name.
a. (Z)-4-ethylhept-3-ene
b. (E)-3,5,6-trimethyloct-2-ene
c. (Z)-2-bromo-1-iodohex-1-ene
Short Answer
Answer
Chapter 10: Q.8. (page 390)
Question: Draw the structure corresponding to each IUPAC name.
a. (Z)-4-ethylhept-3-ene
b. (E)-3,5,6-trimethyloct-2-ene
c. (Z)-2-bromo-1-iodohex-1-ene
Answer
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Get started for freeQuestion: Although naturally occurring unsaturated fatty acids generally have the Z configuration, elaidic acid, a C18 fatty acid having an E double bond, is present in processed foods such as margarine and cooking oils. Predict how the melting point of elaidic acid compares with the melting points of stearic and oleic acids (Table 10.2).
Question: Linolenic acid (Table 10.2) and stearidonic acid are omega-3 fatty acids, unsaturated fatty acids that contain the first double bond located at C3, when numbering begins at the methyl end of the chain. Predict how the melting point of stearidonic acid compares with the melting points of linolenic and stearic acids. A current avenue of research is examining the use of soybean oil enriched in stearidonic acid as a healthier alternative to vegetable oils that contain fewer degrees of unsaturation.
Question: a. What product(s) are formed when the E isomer of C6H5CH=CHC6H5is treated with Br2 , followed by one equivalent of KOH? Label the resulting alkene(s) as E or Z. b. What product(s) are formed when the Z isomer of C6H5CH=CHC6H5 is subjected to the same reaction sequence? c. How are the compounds in parts (a) and (b) related to each other?
Question: Draw a stepwise mechanism for the following reaction.
Question: Draw a stepwise mechanism that shows how all three alcohols are formed from the bicyclic alkene.
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