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Consider the reaction below to answer the following question(s). Consider the reaction below to answer the following question(s). -Refer to instructions. Write the complete stepwise mechanism for this reaction. Show intermediate structures and all electron flow with arrows. -Refer to instructions. Write the complete stepwise mechanism for this reaction. Show intermediate structures and all electron flow with arrows.

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Provide IUPAC names for the structures in the following question(s). -Name: Provide IUPAC names for the structures in the following question(s). -Name:

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trans-but-...

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The two spectra below belong to acetic acid (ethanoic acid) and its isomer, methyl formate (methyl methanoate). Which spectrum corresponds to which compound? Explain your answer. The two spectra below belong to acetic acid (ethanoic acid) and its isomer, methyl formate (methyl methanoate). Which spectrum corresponds to which compound? Explain your answer. (Spectra obtained from SDBSWeb: http://www.aist.go.jp/RIODB/SDBS) The two spectra below belong to acetic acid (ethanoic acid) and its isomer, methyl formate (methyl methanoate). Which spectrum corresponds to which compound? Explain your answer. (Spectra obtained from SDBSWeb: http://www.aist.go.jp/RIODB/SDBS) (Spectra obtained from SDBSWeb: http://www.aist.go.jp/RIODB/SDBS)

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Both of these compounds contain two diff...

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What is the major organic product produced by the following reaction? What is the major organic product produced by the following reaction?

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Tell which spectroscopic technique you would use to distinguish between the two members of the pair. Tell what differences you would expect to see. -Identify spectroscopic technique: Tell which spectroscopic technique you would use to distinguish between the two members of the pair. Tell what differences you would expect to see. -Identify spectroscopic technique:

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IR
1735 cm−1

(alip...

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Draw the major product of the following reaction. Draw the major product of the following reaction.

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11eab600_082c_cbac_9625_233568ed6b14_TB6688_00

What is the IUPAC name of the following compound? What is the IUPAC name of the following compound? A) dimethylamino 3-phenylpropanoic acid B) N,N-dimethyl 2-phenylethyl amide C) N,N-dimethyl 3-phenylpropanamide D) dimethyl 2-phenylpropanoylamine


A) dimethylamino 3-phenylpropanoic acid
B) N,N-dimethyl 2-phenylethyl amide
C) N,N-dimethyl 3-phenylpropanamide
D) dimethyl 2-phenylpropanoylamine

E) None of the above
F) A) and B)

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C

What is the correct assignment of the functional groups in the following compounds? What is the correct assignment of the functional groups in the following compounds? A) 1 = acid chloride; 2 = ester; 3 = nitrile B) 1 = carboxylic acid; 2 = ester; 3 = imide C) 1 = acid chloride; 2 = ester; 3 = amide D) 1 = acid anhydride; 2 = ester; 3 = imide


A) 1 = acid chloride; 2 = ester; 3 = nitrile
B) 1 = carboxylic acid; 2 = ester; 3 = imide
C) 1 = acid chloride; 2 = ester; 3 = amide
D) 1 = acid anhydride; 2 = ester; 3 = imide

E) B) and D)
F) A) and B)

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Which of the following compounds is a 2° amide?


A)
Which of the following compounds is a 2° amide? A) B) C) D)
B)
Which of the following compounds is a 2° amide? A) B) C) D)
C)
Which of the following compounds is a 2° amide? A) B) C) D)
D)
Which of the following compounds is a 2° amide? A) B) C) D)

E) A) and C)
F) All of the above

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Consider the information below to answer the following question(s). The reaction of a carboxylic acid with an alcohol in the presence of acid is termed a Fischer esterification. Consider the information below to answer the following question(s). The reaction of a carboxylic acid with an alcohol in the presence of acid is termed a Fischer esterification. -Refer to instructions. What would be the identity of A, B and C needed to produce the following compound? -Refer to instructions. What would be the identity of A, B and C needed to produce the following compound? Consider the information below to answer the following question(s). The reaction of a carboxylic acid with an alcohol in the presence of acid is termed a Fischer esterification. -Refer to instructions. What would be the identity of A, B and C needed to produce the following compound?

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Provide IUPAC names for the structures in the following question(s). -Name: Provide IUPAC names for the structures in the following question(s). -Name:

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N-cyclopen...

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Draw the structure of polymer formed in the following reaction. Show only a single monomer. Draw the structure of polymer formed in the following reaction. Show only a single monomer.

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Which of the following best describes the key mechanistic steps in the reaction of an acid chloride and an alcohol to form an ester?


A) elimination followed by addition
B) addition followed by decarboxylation
C) addition followed by elimination
D) substitution followed by addition

E) A) and D)
F) A) and C)

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Tell which spectroscopic technique you would use to distinguish between the two members of the pair. Tell what differences you would expect to see. -Identify spectroscopic technique: Tell which spectroscopic technique you would use to distinguish between the two members of the pair. Tell what differences you would expect to see. -Identify spectroscopic technique:

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IR
1820, 1760 cm−1
...

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Draw the major product of the following reaction (which affords a penicillin derivative). Draw the major product of the following reaction (which affords a penicillin derivative).

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Rank the following compounds in order of increasing reactivity with a nucleophile. Rank the following compounds in order of increasing reactivity with a nucleophile.

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Provide the missing structure(s) or reagent(s) for each reaction or sequences of reactions. Show all relevant stereochemistry. -Provide missing structure(s): Provide the missing structure(s) or reagent(s) for each reaction or sequences of reactions. Show all relevant stereochemistry. -Provide missing structure(s):

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Consider the reaction below to answer the following question(s) . Consider the reaction below to answer the following question(s) . -Refer to instructions. This reaction is an example of: A) an intermolecular nucleophilic acyl substitution reaction B) an intramolecular nucleophilic acyl substitution reaction C) an intermolecular S<sub>N</sub>2 reaction D) an intramolecular S<sub>N</sub>2 reaction -Refer to instructions. This reaction is an example of:


A) an intermolecular nucleophilic acyl substitution reaction
B) an intramolecular nucleophilic acyl substitution reaction
C) an intermolecular SN2 reaction
D) an intramolecular SN2 reaction

E) A) and B)
F) A) and C)

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B

What is the correct structure for phenylbenzoate?


A)
What is the correct structure for phenylbenzoate? A) B) C) D)
B)
What is the correct structure for phenylbenzoate? A) B) C) D)
C)
What is the correct structure for phenylbenzoate? A) B) C) D)
D)
What is the correct structure for phenylbenzoate? A) B) C) D)

E) A) and C)
F) All of the above

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Provide the missing structure(s) or reagent(s) for each reaction or sequences of reactions. Show all relevant stereochemistry. -Provide missing structure(s): Provide the missing structure(s) or reagent(s) for each reaction or sequences of reactions. Show all relevant stereochemistry. -Provide missing structure(s):

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