I am stuck on E and B please help Remember to specify stereochemistry in the nam

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I am stuck on E and B please help

Remember to specify stereochemistry in the name when appropriate. When the hydroxyl group is a substituent attached directly to a ring carbon of a cycloalkane, that carbon is automatically numbered and you do not need to specify the locant of the hydroxyl group. Please use the common name tert-butyl instead of 1, 1-dimethylethyl when it is encountered below. Answer key is coded with both the "old-fashioned" and "new-fangle" conventions. Write the IUPAC substitutive name for a. Write the IUPAC substitutive name for b. Write the IUPAC substitutive name for c. Is the conformation of c the most stable one? yes no Write the IUPAC substitutive name for d. Is the conformation of d the most stable one? yes no

Explanation / Answer

B) IUPAC name is 3-cylcohexyl propanol                ( OH is higher priority funtional group and hence it should come under parent chain name , hence main chain is propane and substituent is cylcohexyl)

E) cis-4-tertiary butyl-1-chloro cyclohexane      ( Cl is higher preffered substituent hence numbering starts there and based on alphabetical order butyl comes before chloro)

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