Pharmaceutical Chemistry Question Paper MCQ - 4



Q. No. 31. Which of the following statements regarding the E1 
                  mechanism is wrong?
Option A Reactions by the E1 mechanism are unimolecular in the 
                 rate-determining step
Option B Reactions by the E1 mechanism are generally first order
Option C Reactions by the E1 mechanism usually occur in one step
Option D Reactions by the E1 mechanism are multi-step reactions

Correct Option C

Q. No. 32. Which of the following statements regarding the E2 mechanism is wrong?
Option A Reactions by the E2 mechanism are always bimolecular
Option B Reactions by the E2 mechanism are generally second 
                 order
Option C Reactions by the E2 mechanism usually occur in one step
Option D Reactions by the E2 mechanism usually occur in two 
                 steps

Correct Option D

Q. No. 33.Which of the following statements regarding 
                 mechanisms of elimination reaction is wrong?
Option A The E1 mechanism does not require a base
Option B The E2 mechanism generally occurs under highly basic 
                 conditions
Option C The E2 mechanism is stereospecific
Option D The E1cB mechanism is usually unimolecular in the rate-
                determining step but leads to a second order rate law

Correct Option A

Q. No. 34. Stereoisomers differ from each other in what 
                  respect?
Option A Composition
Option B Constitution
Option C Configuration
Option D Steric hindrance

Correct Option C

Q. No. 35. Which of the following statements is not correct?
Option A a pair of enantiomeric compounds will have the same 
                melting point
Option B a pair of enantiomeric compounds will have the same 
                solubility in ethanol
Option C a pair of enantiomeric compounds will have exactly the 
                 same functional groups
Option D a pair of enantiomeric compounds will have identical 
                 optical rotations

Correct Option D

Q. No. 36. What common symmetry elements if any are found in the stable chair conformer of trans-1,2-dichlorocyclohexane?
Option A A single mirror plane and a C2 rotational axis
Option B A single mirror plane and a C3 rotational axis
Option C Two orthogonal mirror planes and a C2 rotational axis
Option D A single C2 rotational axis but no mirror plane

Correct Option D

Q. No. 38. Which of the following statements must be true for 
                   two pure chiral isomers ?
Option A They must be enantiomers
Option B They must be diastereomers
Option C They must be stereoisomers
Option D They must be optically active

Correct Option C

Q. No. 39. Which of the following compounds has no isomer?
Option A CH3CH2CH2Cl
Option B CH3CHO
Option C CH2=CHCl
Option D ClCH2CH2Cl

Correct Option C

Q. No. 40. Which of the following series contain a free radical,                      a nucleophile and an electrophile?
Option A Br- BF3NH3
Option B NH3 NO2+  Br2
Option C H2O ClNH3
Option D Cl2 CH4 NH3

Correct Option A