Questions from Organic Chemistry


Q: Draw a structure for each of the following ions; in each

Draw a structure for each of the following ions; in each case, indicate which atom possesses the formal charge: a. BH4– b. NH2– c. C2H5+

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Q: 74. What is the configuration of the stereocenter in the following

74. What is the configuration of the stereocenter in the following compound? a. R b. S c. Z d. Depends on T 75. What is the relationship between the following two compounds? a. Enantiomers b. D...

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Q: (S)-1-Bromo-1,2-diphenylethane

(S)-1-Bromo-1,2-diphenylethane reacts with a strong base to produce cis-stilbene and trans-stilbene: a. This reaction is stereoselective, and the major product is transstilbene. Explain why the trans...

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Q: Which of the following reactions is expected to produce 1-propanol

Which of the following reactions is expected to produce 1-propanol (CH3CH2CH2OH) at a faster rate? Explain.

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Q: Therearetwostereoisomersof1-tert-butyl-4-chloro-cyclohexane.

Therearetwostereoisomersof1-tert-butyl-4-chloro-cyclohexane. One of these isomers reacts with sodium ethoxide in an E2 reaction that is 500 times faster than the reaction of the other isomer. Identify...

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Q: In 2010 the structure of the compound (+)-trigonoliimine A (isolated

In 2010 the structure of the compound (+)-trigonoliimine A (isolated from the leaves of a plant in the Yunnan province of China) was reported as shown below. In 2011, a synthesis of the reported struc...

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Q: Substitution vs. Elimination: Identify the major and minor product(

Substitution vs. Elimination: Identify the major and minor product(s) for each of the following reactions:

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Q: 77. All of the following are significant resonance structures of the

77. All of the following are significant resonance structures of the phenyl carbocation, EXCEPT: 78. Which of the following resonance structures is the greatest contributor to the resonance hybrid?...

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Q: Predict the major product for each of the following reactions.

Predict the major product for each of the following reactions.

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Q: Consider the following substitution reaction: / a.

Consider the following substitution reaction: a. Determine whether this reaction proceeds via an SN2 or SN1 process, and draw a complete mechanism. b. What is the expected rate equation for this pro...

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