7) Select the best reagent (or set of reagents) to accomplish the following transformation.

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**Page 2 of 7**

**7) Select the best reagent (or set of reagents) to accomplish the following transformation.**

Diagram: Shows a cyclohexane ring with a propyl group attached to it and a question mark indicating a transformation to a cyclohexane ring with a methoxy group.

Options:
a) NaOCH3 
b) NaOH, H2O 
c) H2O, H2SO4 
d) CH3OH, H2SO4

---

**8) Select the major product(s) of the following reaction.**

Diagram: A cyclohexene ring with a methyl group undergoing hydrogenation with H2(g) over palladium on carbon (Pd/C).

Options:
a) Cyclohexane with a chiral center.
b) Cyclohexane with a different chiral center.
c) Cyclohexane.
d) Mixture of two chiral cyclohexanes.

---

**9) Select the structure formed by the reaction step shown below.**

Diagram: A cyclohexane ring with a dibromide group, with a dotted arrow indicating a potential formation of an intermediate.

Options:
a) Cyclohexane with a bromonium ion.
b) Cyclohexane with a bromine cation.
c) Cyclohexane with two bromine cations.
d) Cyclohexane with a bromonium ion from a different pathway.

---

**10) What is the IUPAC name of the following compound?**

Diagram: A hexane structure with a hydroxyl group and a chlorine substituent.

Options:
a) (S)-3-chloro-5,5-dimethylhexan-1-ol
b) (R)-3-chloro-5,5-dimethylhexan-1-ol
c) (R)-4-chloro-2,2-dimethylhexan-6-ol
d) (S)-4-chloro-2,2-dimethylhexan-6-ol

---

**11) Which alkene would you treat with a peroxyacid to obtain the following epoxide?**

Diagram: An epoxide structure indicated with hydrogen atoms on each carbon.

Options:
a) Linear alkene with four carbons.
b) Linear alkene with six carbons.
c) Branched alkene with four carbons.
d) Cyclic alk
Transcribed Image Text:**Page 2 of 7** **7) Select the best reagent (or set of reagents) to accomplish the following transformation.** Diagram: Shows a cyclohexane ring with a propyl group attached to it and a question mark indicating a transformation to a cyclohexane ring with a methoxy group. Options: a) NaOCH3 b) NaOH, H2O c) H2O, H2SO4 d) CH3OH, H2SO4 --- **8) Select the major product(s) of the following reaction.** Diagram: A cyclohexene ring with a methyl group undergoing hydrogenation with H2(g) over palladium on carbon (Pd/C). Options: a) Cyclohexane with a chiral center. b) Cyclohexane with a different chiral center. c) Cyclohexane. d) Mixture of two chiral cyclohexanes. --- **9) Select the structure formed by the reaction step shown below.** Diagram: A cyclohexane ring with a dibromide group, with a dotted arrow indicating a potential formation of an intermediate. Options: a) Cyclohexane with a bromonium ion. b) Cyclohexane with a bromine cation. c) Cyclohexane with two bromine cations. d) Cyclohexane with a bromonium ion from a different pathway. --- **10) What is the IUPAC name of the following compound?** Diagram: A hexane structure with a hydroxyl group and a chlorine substituent. Options: a) (S)-3-chloro-5,5-dimethylhexan-1-ol b) (R)-3-chloro-5,5-dimethylhexan-1-ol c) (R)-4-chloro-2,2-dimethylhexan-6-ol d) (S)-4-chloro-2,2-dimethylhexan-6-ol --- **11) Which alkene would you treat with a peroxyacid to obtain the following epoxide?** Diagram: An epoxide structure indicated with hydrogen atoms on each carbon. Options: a) Linear alkene with four carbons. b) Linear alkene with six carbons. c) Branched alkene with four carbons. d) Cyclic alk
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