Draw the structure corresponding to each IUPAC name. How is the difference between cis and trans for organic chem?

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Draw the structure corresponding to each IUPAC name. How is the difference between cis and trans for organic chem?
The image contains a list of chemical compound names, aligned vertically and separated by dotted lines. The following are the transcriptions of the compounds:

1. **e. (Z)-2-bromo-1-iodo-1-hexene**
2. **f. cis-4-methyl-2-pentene**
3. **g. (Z)-4-ethyl-3-heptene**
4. **h. (E)-3,5,6-trimethyl-2-octene**

Each compound name describes specific structural isomers with their respective prefixes indicating stereochemistry, such as (Z) and (E), as well as substituents like bromo, iodo, methyl, and ethyl.
Transcribed Image Text:The image contains a list of chemical compound names, aligned vertically and separated by dotted lines. The following are the transcriptions of the compounds: 1. **e. (Z)-2-bromo-1-iodo-1-hexene** 2. **f. cis-4-methyl-2-pentene** 3. **g. (Z)-4-ethyl-3-heptene** 4. **h. (E)-3,5,6-trimethyl-2-octene** Each compound name describes specific structural isomers with their respective prefixes indicating stereochemistry, such as (Z) and (E), as well as substituents like bromo, iodo, methyl, and ethyl.
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