Correct Answer
verified
Essay
Correct Answer
verified
Multiple Choice
A) H2SO4
B) H2O
C) NaOCH3
D) KOtBu
Correct Answer
verified
Multiple Choice
A) F−
B) Cl−
C) Br−
D) I−
Correct Answer
verified
Essay
Correct Answer
verified
Essay
Correct Answer
verified
Multiple Choice
A) Rate = k [i-PrBr]
B) Rate = k [i-PrBr]2
C) Rate = k [CH3OH]
D) Rate = k [i-PrBr][CH3OH]
Correct Answer
verified
Multiple Choice
A) A carbocation intermediate is formed.
B) The mechanism has only one step.
C) Aprotic solvents are good choices for SN1 reactions.
D) The stereochemical outcome is inversion at the carbon bearing the leaving group.
Correct Answer
verified
Essay
Correct Answer
verified
Multiple Choice
A) The heterolysis of a bond between atoms which do not bear formal charges always produces a cation and an anion
B) The charged carbon atom of a carbocation has a complete octet of valence shell electrons
C) Carbocations are Lewis acids
D) Nucleophiles seek centers of low electron density
Correct Answer
verified
Multiple Choice
A) Rate = k [i-PrBr]
B) Rate = k [i-PrBr]2
C) Rate = k [NaOCH3]
D) Rate = k [i-PrBr][NaOCH3]
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
Correct Answer
verified
Multiple Choice
A) (R) 2-cyanohexane
B) (S) 2-cyanohexane
C) 1-hexene
D) 2-hexene
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
Correct Answer
verified
Multiple Choice
A) Rate = k [BuCl]
B) Rate = k [BuCl][NaI]
C) Rate = k [NaI]
D) Rate = k [BuCl]2
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
Correct Answer
verified
Multiple Choice
A) 1-hexyne
B) 2-hexyne
C) propene + propyne
D) propane + propyne
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
Correct Answer
verified
Showing 1 - 20 of 104
Related Exams