Draw the structure of (Z)-3-bromo-6-methyl-2-heptene. Be sure the stereochemistry is drawn clearly

Draw the skeletal (line-bond) structure for (S)-2-hydroxypentan-3-one. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.

Draw the skeletal (line-bond) structure of (R)-1-ethyl-3-ethynylcyclohex-1-ene. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.

Identify the reactants and products for the following reaction. Include predicted stereochemistry. (R)-2-butylchloride + CH3S¯→

Question 11

Draw structures for (R)-3-(4-ethylhexyl)cyclobutene and (E)-5-(bromomethyl)dec-5-ene.

5. A compound C10H14 contains two triple bonds and reacts with ozone to form HOOCCH₂CH₂COOH and CH3CH₂COOH in the ratio of 1 to 2. What is the structure of the original compound.

Draw the skeletal (line-bond) structure of (S)-5-chloro-2-methylnon-3-yne. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.

The two alkenes below react with HI at different rates. CH3CH=CHCH3 and CH₂=CH₂ Draw the structural formula of the MAJOR product formed by the alkene having the HIGHER reaction rate. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. TAYY [ ] در ChemDoodle Ⓡ