Objective Questions
All objective questions for CHM 102
Questions (1999)
| # | Question | Topic | Actions |
|---|---|---|---|
| 201 |
How many equivalents of H2 are required to fully hydrogenate an alkyne to an al…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 202 |
What is the product of ozonolysis (O3 followed by H2O) of 2-butyne (CH3C≡CCH3)?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 203 |
Why do alkynes react with bromine (Br2) but alkanes do not under normal conditi…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 204 |
What is the product when propyne (CH3C≡CH) reacts with one equivalent of HBr?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 205 |
Which of the following bases is strong enough to deprotonate a terminal alkyne …
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 206 |
What is the common name for propyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 207 |
What type of hybridization change occurs when an alkyne is hydrogenated to an a…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 208 |
What is the product of the reaction of sodium acetylide (HC≡CNa) with 1-bromopr…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 209 |
Which of the following alkynes is also known as dimethylacetylene?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 210 |
What is the product when 2-butyne is treated with excess Br2?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 211 |
Which of the following is a valid method to prepare an alkyne from a vicinal di…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 212 |
What is the product of the reaction of ethylmagnesium bromide (CH3CH2MgBr) with…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 213 |
What is the IUPAC name for HC≡C-CH2-CH3?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 214 |
Why are internal alkynes generally more stable than terminal alkynes?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 215 |
What is the product when a terminal alkyne is treated with Cu2Cl2 in NH4OH?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 216 |
What is the molecular formula of a cyclic alkyne with 5 carbons?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 217 |
Which of the following reactions is used to synthesize higher alkynes from lowe…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 218 |
What is the boiling point trend of alkynes compared to alkanes of similar molec…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 219 |
What is the common name for HC≡C-CH2-CH2-CH3?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 220 |
What is the product of the reaction of 2-butyne with H2/Lindlar's catalyst?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 221 |
What type of compound is formed when an alkyne undergoes ozonolysis with reduct…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 222 |
What is the key difference in reactivity between terminal and internal alkynes …
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 223 |
What is the pKa of water compared to a terminal alkyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 224 |
What is the major product of the addition of one equivalent of HCl to propyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 225 |
What is the major product when 2-butyne is hydrated with HgSO4/H2SO4?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 226 |
Which of the following is a test for unsaturation that alkynes fail to pass?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 227 |
What is the structure of a vicinal dihalide used to prepare an alkyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 228 |
Which statement about the carbon-carbon triple bond is FALSE?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 229 |
What is the functional group of an amine?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 230 |
What is the IUPAC name for CH3CH2CH2NH2?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 231 |
Which of the following is a secondary amine?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 232 |
What is the common name for (CH3)3N?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 233 |
What type of amine is aniline (C6H5NH2)?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 234 |
Which method involves the reaction of an alkyl halide with excess ammonia to fo…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 235 |
For the ammonolysis of alkyl halides to proceed efficiently via SN2, the alkyl …
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 236 |
What is the product of the reduction of a nitrile (R-C≡N) with LiAlH4?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 237 |
Reduction of nitroalkanes (R-NO2) with Sn/HCl produces:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 238 |
Which reagent is commonly used to reduce amides to amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 239 |
The carbylamine test (isocyanide test) is used to detect:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 240 |
In the carbylamine reaction, what is the product when methylamine reacts with C…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 241 |
What type of hybridization does the nitrogen atom have in a typical amine?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 242 |
Which of the following amines has the highest boiling point for a similar molec…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 243 |
Why are amines soluble in water?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 244 |
What is the product when a primary amine reacts with nitrous acid (HNO2)?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 245 |
What is the product when a secondary aliphatic amine reacts with nitrous acid (…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 246 |
Tertiary aliphatic amines react with nitrous acid to form:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 247 |
Why are aliphatic amines stronger bases than aromatic amines like aniline?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 248 |
Which of the following is the strongest base?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 249 |
What is the approximate pKb range for aliphatic amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 250 |
What is the product of the reaction between an amine and a carboxylic acid?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 251 |
What is the IUPAC name for (CH3CH2)2NH?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 252 |
In the Gabriel synthesis, phthalimide is used to prepare:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 253 |
What is the product of exhaustive methylation of a tertiary amine with excess C…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 254 |
Which of the following is NOT a typical physical property of amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 255 |
What is the Hofmann elimination?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 256 |
Which reducing agent is commonly used in reductive amination of aldehydes/keton…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 257 |
In reductive amination, a ketone reacts with a primary amine to form, after red…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 258 |
What is the smell associated with most amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 259 |
Which of the following correctly orders boiling points for similar molecular we…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 260 |
Why are aromatic amines weaker bases than aliphatic amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 261 |
Which substituent on aniline would increase its basicity?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 262 |
What is the product of the reaction of ethylamine with HCl?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 263 |
The reaction of an amine with an acid chloride yields:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 264 |
Which of the following amines is a gas at room temperature?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 265 |
What is the IUPAC name for C6H5-NH-CH3?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 266 |
Quaternary ammonium salts have the general formula:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 267 |
What is the common name for CH3CH2NH2?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 268 |
Which of the following statements about amine basicity is TRUE?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 269 |
What is the product when a 1° amine is treated with excess CH3I (methyl iodide)?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 270 |
What is the functional group interconversion in the reduction of an amide with …
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 271 |
Which of the following is an example of a heterocyclic amine?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 272 |
What is the major product when a tertiary amine oxide is heated?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 273 |
Which of the following is NOT a method of preparing primary amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 274 |
What is the product when an aromatic primary amine (aniline) is treated with ni…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 275 |
Which of the following is the strongest base in aqueous solution?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 276 |
What is the pKb of ammonia?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 277 |
Which of the following is a 4° (quaternary) ammonium salt?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 278 |
In the Gabriel synthesis, which reagent is used to alkylate phthalimide?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 279 |
What is the product of the reaction between an aliphatic primary amine and chlo…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 280 |
Secondary and tertiary amines can be distinguished from primary amines by:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 281 |
What is the common name for (CH3)2CH-NH2?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 282 |
Which functional group is produced when a primary amine reacts with a ketone in…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 283 |
Which of the following amines will NOT react with Hinsberg reagent (benzenesulf…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 284 |
What is the product of Hofmann degradation (Hofmann rearrangement) of an amide?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 285 |
Which of the following is a quaternary ammonium hydroxide that upon heating und…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 286 |
What is the characteristic odor of isocyanides (carbylamines)?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 287 |
Which of the following correctly represents the basicity order of amines in aqu…
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 288 |
Which of the following is NOT a carboxylic acid derivative?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 289 |
What is the general reaction mechanism for carboxylic acid derivatives?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 290 |
What is the IUPAC name for CH3CH2COCl?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 291 |
Which reagent is commonly used to convert a carboxylic acid into an acid chlori…
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 292 |
What is the product of the reaction of a carboxylic acid with PBr3?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 293 |
How is a symmetrical acid anhydride prepared from a carboxylic acid?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 294 |
What is the common name for CH3COOCH2CH3?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 295 |
What is the IUPAC name for methyl propanoate?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 296 |
In ester nomenclature, the name consists of:
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 297 |
What is the product of the reaction of an acid chloride with NH3?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 298 |
What is the product when an acid chloride reacts with a primary amine (RNH2)?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 299 |
What is the IUPAC name for benzoyl chloride (C6H5COCl)?
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |
| 300 |
What is the product of the reaction of an acid chloride with an alcohol in the …
|
Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions | View |