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

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

Chemistry
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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Parase help me solve any problem on this page I need help particularly understanding the mechanisms

**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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