

McqMate
These multiple-choice questions (MCQs) are designed to enhance your knowledge and understanding in the following areas: Bachelor of Pharmacy (B. Pharma) , Pharmacy .
101. |
Which is the most reactive five membered heterocyclic compound? |
A. | Pyrrole |
B. | Furan |
C. | Thiophene |
D. | Pyridine |
Answer» A. Pyrrole |
102. |
What is the product when thiophene reacts with Br2 in benzene? |
A. | 2-bromothiophene |
B. | 3-bromothiophene |
C. | 2,5-dibromothiophene |
D. | 3,4-dibromothiophene |
Answer» C. 2,5-dibromothiophene |
103. |
What is the product when pyrrole reacts with Br2 in ethanol? |
A. | 2,3-dibromopyrrole |
B. | 2,3,4,5-tetrabromopyrrole |
C. | 2,5-dibromopyrrole |
D. | 3,4-dibromopyrrole |
Answer» B. 2,3,4,5-tetrabromopyrrole |
104. |
What is the name of the following reaction? |
A. | Gattermann reaction |
B. | Riemer tiemann reaction |
C. | Friedal craft reaction |
D. | Blanc’s chloromethylation |
Answer» B. Riemer tiemann reaction |
105. |
What is the name of the following reaction? |
A. | Gattermann reaction |
B. | Riemer tiemann reaction |
C. | Friedal craft reaction |
D. | Blanc’s chloromethylation |
Answer» A. Gattermann reaction |
106. |
What will be the reagent used for the completion of the following reaction? |
A. | Concentrated acid |
B. | Dilute acid |
C. | Concentrated base |
D. | Dilute base |
Answer» B. Dilute acid |
107. |
Which heteroatom present in pyrrole? |
A. | Oxygen |
B. | Nitrogen |
C. | Silicon |
D. | Sulphur |
Answer» B. Nitrogen |
108. |
Which heteroatom present in Furan? |
A. | Oxygen |
B. | Nitrogen |
C. | Silicon |
D. | Sulphur |
Answer» A. Oxygen |
109. |
Which heteroatom present in thiophene? |
A. | Nitrogen |
B. | Silicon |
C. | Oxygen |
D. | Sulphur |
Answer» D. Sulphur |
110. |
Which compound is most basic? |
A. | Pyridine |
B. | Pyrrole |
C. | Imidazole |
D. | Pyrrolidine |
Answer» C. Imidazole |
111. |
Which is least basic compound? |
A. | Pyridine |
B. | Pyrrole |
C. | Imidazole |
D. | Pyrrolidine |
Answer» B. Pyrrole |
112. |
Which of the following solvents is a heterocyclic compound? |
A. | DMSO |
B. | DMF |
C. | THF |
D. | None of the above |
Answer» C. THF |
113. |
Which of the followings statements is correct? |
A. | Pyrrole has less aromatic character than furan |
B. | Pyridine is isoelectronic with benzene |
C. | Pyridine is tertiary amine |
D. | Pyrrole is strong base |
Answer» C. Pyridine is tertiary amine |
114. |
What is the correct order of reactivity (most reactive first) of pyrrole, furan and thiophene towards electrophiles? |
A. | Furan > Pyrrole > Thiophene |
B. | Pyrrole > Furan > Thiophene |
C. | Furan > Thiophene > Pyrrole |
D. | Thiophene > Pyrrole > Furan |
Answer» B. Pyrrole > Furan > Thiophene |
115. |
Electrophilic substitution in furan usually occurs at: |
A. | Both the C2 and C3 atom |
B. | The O atom |
C. | The C2 atom |
D. | The C3 atom |
Answer» C. The C2 atom |
116. |
Nitration of pyrrole is best carried out using: |
A. | Acetyl nitrate |
B. | Ammonium nitrate |
C. | Concentrated nitric and sulphuric acid |
D. | Nitric acid |
Answer» A. Acetyl nitrate |
117. |
If you wanted to form 2,3,4,5-tetrabromopyrrole from pyrrole, which of the following conditions would be the best choice? |
A. | Br2 at 273K |
B. | Br2 at298 K |
C. | Br2 in the presence of radical initiator |
D. | Br2 in the presence of Lewis acid |
Answer» C. Br2 in the presence of radical initiator |
118. |
Which statement about thiophene is incorrect? |
A. | The S atom contributes two electrons to the n-system |
B. | Thiophene is polar |
C. | Thiophene is less reactive than pyrrole |
D. | Thiophene is more reactive than furan |
Answer» D. Thiophene is more reactive than furan |
119. |
Pyrrole undergoes sulfonation in presence of _______to produce pyrrole – 2 – sulfonic acid. |
A. | Conc. Sulphuric acid |
B. | SO3 and pyridine |
C. | Dilute sulphuric acid/pyridine |
D. | SO3 and ethanol |
Answer» B. SO3 and pyridine |
120. |
Pyrrole undergoes iodination in presence of Iodine and potassium iodide to produce_____. |
A. | 2 – iodo pyrrole |
B. | 3 – iodo pyrrole |
C. | Tetra iodo pyrrole |
D. | Tri iodo pyrrole |
Answer» C. Tetra iodo pyrrole |
121. |
Oxidation of pyrrole in presence of chromium oxide (Cr2O3) and acetic acid produce_______. |
A. | Maleinimide |
B. | Maleic acid |
C. | Pyrrole N-oxide |
D. | None of the above |
Answer» A. Maleinimide |
122. |
Pyrrole is reduced by using Zn and acetic acid to get product_______ |
A. | 2 – pyrroline |
B. | 3 – pyrroline |
C. | Pyrrolidine |
D. | All of the above |
Answer» B. 3 – pyrroline |
123. |
Which product will be produced when pyrrole undergoes catalytic reduction in presence of hydrogen gas and Ni metal? |
A. | 2 – pyrroline |
B. | 3 – pyrroline |
C. | Pyrrolidine |
D. | All of the above |
Answer» C. Pyrrolidine |
124. |
Identify the given heterocyclic compound. |
A. | Furan |
B. | Pyrazole |
C. | Pyrrole |
D. | Pyridine |
Answer» C. Pyrrole |
125. |
Pyrrole potassium on treatment with CO2 under pressure give mixture of 2 and 3 pyrrole – carboxylic acid, identify the reaction. |
A. | Kolbe-Schmidt reaction |
B. | Reamer-Tiemann reaction |
C. | Gattermann Koch reaction |
D. | Coupling reaction |
Answer» A. Kolbe-Schmidt reaction |
126. |
Pyrrole is heated with_________ to open the ring and form succinaldehyde dioxime. |
A. | Concentrated sulphuric acid |
B. | Strong alkali with pyridine |
C. | Hydrogen cyanide with HCl |
D. | Ethanolic hydroxylamine hydrochloride |
Answer» D. Ethanolic hydroxylamine hydrochloride |
127. |
Atorvastatin, drug useful in CVS disease, contain heterocyclic ring______. |
A. | Pyrazole |
B. | Pyrrole |
C. | Imidazole |
D. | Purine |
Answer» B. Pyrrole |
128. |
Bepridil, calcium channel blocker, contain heterocyclic ring_____ |
A. | Pyrrole |
B. | Purine |
C. | Indole |
D. | Pyridine |
Answer» A. Pyrrole |
129. |
Ondansetron, anti emetic drug, contain heterocyclic ring______. |
A. | Thiophene |
B. | Pyrrole |
C. | Furan |
D. | Pyrimidine |
Answer» B. Pyrrole |
130. |
Which drug(s) possess pyrrole heterocyclic compound from the followings? |
A. | Captopril |
B. | Lincomycin |
C. | Triprolidine |
D. | All of the above |
Answer» D. All of the above |
131. |
Identify the following heterocyclic compound. |
A. | Furan |
B. | Thiophene |
C. | Oxazole |
D. | Thiazole |
Answer» A. Furan |
132. |
Complete the following reaction. |
A. | Pyrrole |
B. | Furan |
C. | Indole |
D. | Oxazole |
Answer» B. Furan |
133. |
Which would be the intermediate in the following reaction? |
A. | Furan – 2 carboxide |
B. | Furan- 2 – carbinol |
C. | Furoic acid |
D. | None of the above |
Answer» C. Furoic acid |
134. |
Which would be the product when furan undergoes sulfonation in the presence of SO3 and pyridine? |
A. | Furan – 2 – sulfolic acid |
B. | Furan – 3 – sulfonic acid |
C. | Mixture of (a) & (b) |
D. | None of the above |
Answer» A. Furan – 2 – sulfolic acid |
135. |
Which reagent is used for the nitration of furan? |
A. | Conc. Nitric acid and sulphuric acid |
B. | Acetyl nitrate |
C. | Nitrobenzene |
D. | Dilute nitric acid with benzene |
Answer» B. Acetyl nitrate |
136. |
Friedel craft acetylation of furan by using acetic anhydride is carried out in the presence of catalyst______. |
A. | AlCl3 |
B. | FeCl3 |
C. | BF3 |
D. | LIAlH4 |
Answer» C. BF3 |
137. |
Identify the reaction: when furan react with aryl diazonium chloride in the presence of strong alkali to produce 2 – aryl furan. |
A. | Mercuration |
B. | Gattermann Koch reaction |
C. | Kolbe reaction |
D. | Gomberg reaction |
Answer» D. Gomberg reaction |
138. |
Bromination of furan by using Br2 will produce_________. |
A. | 2 – bromo furan |
B. | 3 – bromo furan |
C. | 2,5 – dibromo furan |
D. | None of the above |
Answer» D. None of the above |
139. |
Identify the following reaction: |
A. | Cannizaro reaction |
B. | Benzoin condensation |
C. | Gomberg reaction |
D. | Mercuration |
Answer» A. Cannizaro reaction |
140. |
Identify the following reaction: |
A. | Gomberg reaction |
B. | Reamer tiemann reaction |
C. | Benzoin condensation |
D. | Aldol condensation |
Answer» C. Benzoin condensation |
141. |
Complete the reaction: |
A. | Br2 |
B. | HBr |
C. | KBr in alcohol |
D. | NaBr in pyridine |
Answer» A. Br2 |
142. |
Furan on treatment with acid undergoes protonation and form________. |
A. | Protonated furan |
B. | Polymeric product |
C. | Dihydro furan |
D. | None of the above |
Answer» B. Polymeric product |
143. |
Oxidation of furan produces_________. |
A. | Furan oxide |
B. | Furfural |
C. | Furfuric acid |
D. | Succinaldehyde |
Answer» D. Succinaldehyde |
144. |
Catalytic reduction of furan gives______ |
A. | 2,3 – dihydro furan |
B. | 2,5 – dihydro furan |
C. | Tetra hydro furan |
D. | 3,4 – dihydro furan |
Answer» C. Tetra hydro furan |
145. |
Prazocin, sympatholytic drug contain__________heterocyclic ring. |
A. | Furan |
B. | Pyrrole |
C. | Oxazole |
D. | Indole |
Answer» A. Furan |
146. |
Which drug of following does not contain furan ring? |
A. | Furazolidone |
B. | Lorpiprazole |
C. | Terazocin |
D. | Dantrolene |
Answer» B. Lorpiprazole |
147. |
Amiodarone, antiarrhythmic agent, possess_________ heterocyclic ring. |
A. | Pyridine |
B. | Furan |
C. | Thiophene |
D. | Purine |
Answer» B. Furan |
148. |
From the followings, which drug contain furan heterocyclic ring? |
A. | Furazolidine |
B. | Nitrofurantoin |
C. | Fluticazone |
D. | All of the above |
Answer» D. All of the above |
149. |
Ranitidine, H2 receptor antagonist, possess________heterocyclic ring. |
A. | Acridine |
B. | Azepine |
C. | Pyridine |
D. | Furan |
Answer» D. Furan |
150. |
Pilocarpine, cholinergic agonist, contains________heterocyclic ring. |
A. | Furan |
B. | Pyrrole |
C. | Thiophene |
D. | Purine |
Answer» A. Furan |
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