Filters
Question type
Study Flashcards

Which of the following conditions and reagents were used to make this compound? Which of the following conditions and reagents were used to make this compound? A) B) C) D) E)


A) Which of the following conditions and reagents were used to make this compound? A) B) C) D) E)
B) Which of the following conditions and reagents were used to make this compound? A) B) C) D) E)
C) Which of the following conditions and reagents were used to make this compound? A) B) C) D) E)
D) Which of the following conditions and reagents were used to make this compound? A) B) C) D) E)
E) Which of the following conditions and reagents were used to make this compound? A) B) C) D) E)

F) C) and E)
G) C) and D)

Correct Answer

verifed

verified

which product will be observed? which product will be observed? A) B) C) D) E)


A) which product will be observed? A) B) C) D) E)
B) which product will be observed? A) B) C) D) E)
C) which product will be observed? A) B) C) D) E)
D) which product will be observed? A) B) C) D) E)
E) which product will be observed? A) B) C) D) E)

F) C) and D)
G) A) and B)

Correct Answer

verifed

verified

Which reagent would you use to accomplish the transformation shown here? Which reagent would you use to accomplish the transformation shown here? A) B) C) D) E)


A) Which reagent would you use to accomplish the transformation shown here? A) B) C) D) E)
B) Which reagent would you use to accomplish the transformation shown here? A) B) C) D) E)
C) Which reagent would you use to accomplish the transformation shown here? A) B) C) D) E)
D) Which reagent would you use to accomplish the transformation shown here? A) B) C) D) E)
E) Which reagent would you use to accomplish the transformation shown here? A) B) C) D) E)

F) A) and B)
G) A) and C)

Correct Answer

verifed

verified

Draw the product of the following transformation: Draw the product of the following transformation:

Correct Answer

verifed

verified

Provide the missing reagents in the following reaction sequence. Provide the missing reagents in the following reaction sequence.

Correct Answer

verifed

verified

Predict the product of the following transformation, including the correct stereochemistry. Predict the product of the following transformation, including the correct stereochemistry.

Correct Answer

verifed

verified

List three ways to accomplish the transformation shown here. List three ways to accomplish the transformation shown here.

Correct Answer

verifed

verified

H2(g) with a metal catalyst suc...

View Answer

Devise a multistep synthesis of the target molecule from the given starting material.Show the reagents needed for each step and the product of each step. Devise a multistep synthesis of the target molecule from the given starting material.Show the reagents needed for each step and the product of each step.

Correct Answer

verifed

verified

Devise a multistep synthesis of the target molecule from the given starting material. Show the reagents needed for each step and the product of each step. Devise a multistep synthesis of the target molecule from the given starting material. Show the reagents needed for each step and the product of each step.

Correct Answer

verifed

verified

Which product will be observed? Which product will be observed? A) B) C) D) E) c and d


A) Which product will be observed? A) B) C) D) E) c and d
B) Which product will be observed? A) B) C) D) E) c and d
C) Which product will be observed? A) B) C) D) E) c and d
D) Which product will be observed? A) B) C) D) E) c and d
E) c and d

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

Correct Answer

verifed

verified

Provide the missing reagents and structures. Provide the missing reagents and structures.

Correct Answer

verifed

verified

Starting with an alkene, which of these methods would produce at least one carbonyl compound as the major product? Assume appropriate aqueous workup in all cases.


A) OsO4
B) H3O+
C) H2 and Lindlar's catalyst
D) O3, then H2O2
E) Hg(OAc) 2 and H2O , then NaBH4

F) A) and B)
G) C) and D)

Correct Answer

verifed

verified

The molecule shown was the exclusive product of an ozonolysis reaction followed by a reductive workup.Draw the structures of two possible starting materials that could have been used. The molecule shown was the exclusive product of an ozonolysis reaction followed by a reductive workup.Draw the structures of two possible starting materials that could have been used.

Correct Answer

verifed

verified

Provide two different precursors and the reagents needed to transform them to the compound shown here. Provide two different precursors and the reagents needed to transform them to the compound shown here.

Correct Answer

verifed

verified

Consider alkenes A and B . Consider alkenes A and B . Which of the following is easily accessible from either A or B ? A) B) C) D) E) Both c and d Which of the following is easily accessible from either A or B ?


A) Consider alkenes A and B . Which of the following is easily accessible from either A or B ? A) B) C) D) E) Both c and d
B) Consider alkenes A and B . Which of the following is easily accessible from either A or B ? A) B) C) D) E) Both c and d
C) Consider alkenes A and B . Which of the following is easily accessible from either A or B ? A) B) C) D) E) Both c and d
D) Consider alkenes A and B . Which of the following is easily accessible from either A or B ? A) B) C) D) E) Both c and d
E) Both c and d

F) B) and C)
G) B) and E)

Correct Answer

verifed

verified

Which of the following statements about treatment of an alkyne with sodium metal in ammonia is false? Which of the following statements about treatment of an alkyne with sodium metal in ammonia is false? A) The product of the reaction is a trans alkene. B) A radical anion is protonated by solvent. C) This reaction provides the opposite stereochemistry to that of treating an alkyne with H<sub>2</sub> in the presence of Lindlar's catalyst. D) Sodium amide forms as the reaction proceeds. E) A single electron is donated by sodium to a orbital in the alkyne.


A) The product of the reaction is a trans alkene.
B) A radical anion is protonated by solvent.
C) This reaction provides the opposite stereochemistry to that of treating an alkyne with H2 in the presence of Lindlar's catalyst.
D) Sodium amide forms as the reaction proceeds.
E) A single electron is donated by sodium to a Which of the following statements about treatment of an alkyne with sodium metal in ammonia is false? A) The product of the reaction is a trans alkene. B) A radical anion is protonated by solvent. C) This reaction provides the opposite stereochemistry to that of treating an alkyne with H<sub>2</sub> in the presence of Lindlar's catalyst. D) Sodium amide forms as the reaction proceeds. E) A single electron is donated by sodium to a orbital in the alkyne. orbital in the alkyne.

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

Correct Answer

verifed

verified

Which of the following is not a 1,3-dipolar reagent?


A) Which of the following is not a 1,3-dipolar reagent? A) B) C) D) E)
B) Which of the following is not a 1,3-dipolar reagent? A) B) C) D) E)
C) Which of the following is not a 1,3-dipolar reagent? A) B) C) D) E)
D) Which of the following is not a 1,3-dipolar reagent? A) B) C) D) E)
E) Which of the following is not a 1,3-dipolar reagent? A) B) C) D) E)

F) A) and E)
G) D) and E)

Correct Answer

verifed

verified

Which reagent would you use to accomplish the transformation shown here? Which reagent would you use to accomplish the transformation shown here? A) diazomethane B) bromoform, then potassium tert-butoxide C) trifluoroperacetic acid D) phenylmagnesium bromide in ether, followed by aqueous acid workup E) osmium tetroxide


A) diazomethane
B) bromoform, then potassium tert-butoxide
C) trifluoroperacetic acid
D) phenylmagnesium bromide in ether, followed by aqueous acid workup
E) osmium tetroxide

F) A) and B)
G) A) and E)

Correct Answer

verifed

verified

Devise a multistep synthesis of the target molecule from the given starting material.Show the reagents needed for each step and the product of each step.Assume that the target is racemic; only one enantiomer is shown. Devise a multistep synthesis of the target molecule from the given starting material.Show the reagents needed for each step and the product of each step.Assume that the target is racemic; only one enantiomer is shown.

Correct Answer

verifed

verified

Explain the difference between a heterogeneous catalyst and a homogeneous catalyst.

Correct Answer

verifed

verified

A heterogeneous catalyst is on...

View Answer

Showing 41 - 60 of 65

Related Exams

Exam 1

Atoms and Molecules; Orbitals and Bonding

64 Questions

Exam 2

Alkanes

65 Questions

Exam 3

Alkenes and Alkynes

70 Questions

Exam 4

Stereochemistry

68 Questions

Exam 5

Rings

60 Questions

Exam 6

Substituted Alkanes: Alkyl Halides, Alcohols, Amines, Ethers,thiols, and Thioethers

68 Questions

Exam 7

Substitution Reactions: the Sn2 and Sn1 Reactions

55 Questions

Exam 8

Elimination Reactions: the E1 and E2 Reactions

45 Questions

Exam 9

Analytical Chemistry: Spectroscopy

65 Questions

Exam 10

Electrophilic Additions to Alkenes

68 Questions

Exam 12

Radical Reactions

65 Questions

Exam 13

Dienes and the Allyl System: 2p Orbitals in Conjugation

68 Questions

Exam 14

Aromaticity

66 Questions

Exam 15

Substitution Reactions of Aromatic Compounds

68 Questions

Exam 16

Carbonyl Chemistry 1: Addition Reactions

73 Questions

Exam 17

Carboxylic Acids

66 Questions

Exam 18

Derivatives of Carboxylic Acids: Acyl Compounds

68 Questions

Exam 19

Carbonyl Chemistry 2: Reactions at the Α Position

71 Questions

Exam 20

Special Topic: Carbohydrates

40 Questions

Exam 21

Special Topic: Bio-Organic Chemistry

40 Questions

Exam 22

Special Topic: Amino Acids and Polyamino Acids Peptides and Proteins

39 Questions

Exam 23

Special Topic: Reactions Controlled by Orbital Symmetry

46 Questions

Exam 24

Special Topic: Intramolecular Reactions and Neighboring Group Participation

40 Questions

Show Answer