Objective Questions
All objective questions for CHM 102
Questions (1999)
| # | Question | Topic | Actions |
|---|---|---|---|
| 501 |
Steam distillation is particularly useful for isolating which type of compounds…
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Isolation and Purification of Organic Compounds | View |
| 502 |
Which separation technique is based on the differential solubility of compounds…
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Isolation and Purification of Organic Compounds | View |
| 503 |
Which of the following is NOT a common solvent used in liquid-liquid extraction?
|
Isolation and Purification of Organic Compounds | View |
| 504 |
In column chromatography, the stationary phase is typically which of the follow…
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Isolation and Purification of Organic Compounds | View |
| 505 |
In thin layer chromatography (TLC), what phenomenon causes the solvent to move …
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Isolation and Purification of Organic Compounds | View |
| 506 |
What does Rf stand for in chromatography?
|
Isolation and Purification of Organic Compounds | View |
| 507 |
What is the formula for calculating Rf value in chromatography?
|
Isolation and Purification of Organic Compounds | View |
| 508 |
In recrystallization, a suitable solvent should have which property?
|
Isolation and Purification of Organic Compounds | View |
| 509 |
What is the purpose of recrystallization?
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Isolation and Purification of Organic Compounds | View |
| 510 |
A mixture of chloroform (bp 60°C) and aniline (bp 189°C) can be separated by wh…
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Isolation and Purification of Organic Compounds | View |
| 511 |
Which technique would be most appropriate for separating a mixture of methanol …
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Isolation and Purification of Organic Compounds | View |
| 512 |
The separation of petroleum into gasoline, kerosene, and diesel is achieved by …
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Isolation and Purification of Organic Compounds | View |
| 513 |
In column chromatography, the process of washing the adsorbed compounds off the…
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Isolation and Purification of Organic Compounds | View |
| 514 |
When a mixture is spotted on a TLC plate and developed, the solvent front trave…
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Isolation and Purification of Organic Compounds | View |
| 515 |
Which of the following statements about recrystallization is FALSE?
|
Isolation and Purification of Organic Compounds | View |
| 516 |
In liquid-liquid extraction, the separatory funnel allows separation of two lay…
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Isolation and Purification of Organic Compounds | View |
| 517 |
Which technique would be best for isolating a heat-sensitive natural product fr…
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Isolation and Purification of Organic Compounds | View |
| 518 |
What is the stationary phase in thin layer chromatography (TLC) typically coate…
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Isolation and Purification of Organic Compounds | View |
| 519 |
Which of the following is a common application of extraction in organic chemist…
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Isolation and Purification of Organic Compounds | View |
| 520 |
In a TLC experiment, if the solvent front travels 8 cm and a compound travels 2…
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Isolation and Purification of Organic Compounds | View |
| 521 |
What does a low Rf value indicate in TLC?
|
Isolation and Purification of Organic Compounds | View |
| 522 |
What does a high Rf value indicate in TLC?
|
Isolation and Purification of Organic Compounds | View |
| 523 |
Which of the following is NOT a method of purification or separation?
|
Isolation and Purification of Organic Compounds | View |
| 524 |
In column chromatography, which type of compound elutes first when using a nonp…
|
Isolation and Purification of Organic Compounds | View |
| 525 |
The principle of crystallization relies on the fact that:
|
Isolation and Purification of Organic Compounds | View |
| 526 |
Which chromatographic technique is most useful for quickly checking the purity …
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Isolation and Purification of Organic Compounds | View |
| 527 |
When performing a recrystallization, if crystals do not form upon cooling, what…
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Isolation and Purification of Organic Compounds | View |
| 528 |
In steam distillation, the total vapor pressure equals:
|
Isolation and Purification of Organic Compounds | View |
| 529 |
Which of the following is an advantage of steam distillation over simple distil…
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Isolation and Purification of Organic Compounds | View |
| 530 |
In liquid-liquid extraction, if a compound is more soluble in the organic layer…
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Isolation and Purification of Organic Compounds | View |
| 531 |
What is the name of the glassware used for liquid-liquid extraction?
|
Isolation and Purification of Organic Compounds | View |
| 532 |
Which of the following pairs are commonly separated by simple distillation?
|
Isolation and Purification of Organic Compounds | View |
| 533 |
In chromatography, the mobile phase is:
|
Isolation and Purification of Organic Compounds | View |
| 534 |
In recrystallization, if too much solvent is used, what will happen?
|
Isolation and Purification of Organic Compounds | View |
| 535 |
Filtration is often used in conjunction with which other purification technique?
|
Isolation and Purification of Organic Compounds | View |
| 536 |
Which of the following statements about Rf values is TRUE?
|
Isolation and Purification of Organic Compounds | View |
| 537 |
In distillation, what is the purpose of the condenser?
|
Isolation and Purification of Organic Compounds | View |
| 538 |
What is the purpose of adding boiling chips or stones to a distillation flask?
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Isolation and Purification of Organic Compounds | View |
| 539 |
Which technique would be best for separating a mixture of a solid that sublimes…
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Isolation and Purification of Organic Compounds | View |
| 540 |
In vacuum distillation, the pressure is reduced to:
|
Isolation and Purification of Organic Compounds | View |
| 541 |
Which of the following is an example of a stationary phase in gas chromatograph…
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Isolation and Purification of Organic Compounds | View |
| 542 |
The separation of a mixture of two immiscible liquids can also be achieved by s…
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Isolation and Purification of Organic Compounds | View |
| 543 |
Which of the following is NOT a typical use of separation techniques in organic…
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Isolation and Purification of Organic Compounds | View |
| 544 |
During recrystallization, if colored impurities are present, what can be added …
|
Isolation and Purification of Organic Compounds | View |
| 545 |
Which type of chromatography separates based on molecular size (sieving effect)?
|
Isolation and Purification of Organic Compounds | View |
| 546 |
What is the mobile phase in column chromatography?
|
Isolation and Purification of Organic Compounds | View |
| 547 |
Which of the following is a common drying agent used to remove traces of water …
|
Isolation and Purification of Organic Compounds | View |
| 548 |
The process of converting a solid directly to a gas without passing through the…
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Isolation and Purification of Organic Compounds | View |
| 549 |
How many π bonds are present in a carbon‑carbon triple bond?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 550 |
What is the IUPAC name for CH₃CH₂C≡CH?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 551 |
Why is the C–H bond of a terminal alkyne more acidic than the C–H bonds of alka…
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 552 |
Which reagent is used to test for terminal alkynes by forming a white precipita…
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 553 |
What product is obtained from the reaction of calcium carbide (CaC₂) with water?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 554 |
What type of isomerism exists between 1‑butyne and 2‑butyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 555 |
What is the approximate pKa of a terminal alkyne (e.g., ethyne)?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 556 |
What is the product when 1‑butyne is treated with NaNH₂ in liquid NH₃?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 557 |
Which reaction allows an internal alkyne to be prepared from a terminal alkyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 558 |
What is the major product of the hydration of 1‑butyne (CH₃CH₂C≡CH) with HgSO₄/…
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 559 |
Which catalyst is used for the partial hydrogenation of an alkyne to a cis‑alke…
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 560 |
What is the product when an internal alkyne is reduced with sodium in liquid am…
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 561 |
How many equivalents of H₂ are required to fully hydrogenate an alkyne to an al…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 562 |
What is the product of ozonolysis (O₃ followed by H₂O) of 2‑butyne (CH₃C≡CCH₃)?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 563 |
Why do alkynes react with Br₂ but alkanes do not under normal conditions?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 564 |
What is the major product when propyne (CH₃C≡CH) reacts with one equivalent of …
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 565 |
Which base is strong enough to deprotonate a terminal alkyne (pKa ≈ 25)?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 566 |
What hybridization change occurs when an alkyne is partially hydrogenated to an…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 567 |
What is the product of the reaction of sodium acetylide (HC≡CNa) with 1‑bromopr…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 568 |
Which alkyne is also known as dimethylacetylene?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 569 |
What is the product when 2‑butyne is treated with excess Br₂?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 570 |
Which method is used to prepare an alkyne from a vicinal dihalide?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 571 |
What product is formed when ethylmagnesium bromide (CH₃CH₂MgBr) reacts with pro…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 572 |
What type of precipitate is formed when a terminal alkyne reacts with Cu₂Cl₂ in…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 573 |
What is the molecular formula of a cyclic alkyne with 5 carbons (e.g., cyclopen…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 574 |
Which reaction is used to synthesize higher alkynes from lower alkynes?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 575 |
What is the common name for HC≡C–CH₂–CH₂–CH₃?
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 576 |
What is the product when 2‑butyne is hydrogenated with H₂ / Lindlar’s catalyst?
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Alkynes: Structure, Bonding, and Nomenclature | View |
| 577 |
What is the product when 2‑butyne is reduced with Na/NH₃ (liquid)?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 578 |
What type of products are obtained from the reductive ozonolysis of an alkyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 579 |
Why do only terminal alkynes react with AgNO₃/NH₃?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 580 |
What is the product when acetylene reacts with two equivalents of HBr?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 581 |
Which statement about the carbon–carbon triple bond is FALSE?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 582 |
What is the major product when ethylamine is treated with excess CH₃I?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 583 |
What is the name of the rule that predicts the major product in elimination rea…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 584 |
Which reagent converts an alkene to an aldehyde with one fewer carbon (oxidativ…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 585 |
What stereochemistry results from syn hydroxylation of an alkene with OsO₄?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 586 |
What is the major product from the reaction of 2‑methylpropene with H₂O in the …
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 587 |
What is the common name for (CH₃)₂C=CH₂?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 588 |
What is the name of the rule that predicts the major product of elimination as …
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 589 |
What is the product when an unsymmetrical alkene undergoes anti‑Markovnikov add…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 590 |
What is the product of catalytic hydrogenation of 2‑butene?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 591 |
What is the test for unsaturation that involves decolorization of brown bromine…
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 592 |
What is the 3D shape around the carbon atoms in an alkyne?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 593 |
What is the correct IUPAC name for the compound CH₃CH₂C≡CCH₃?
|
Alkynes: Structure, Bonding, and Nomenclature | View |
| 594 |
What is the functional group present in amines?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 595 |
What is the IUPAC name for CH₃CH₂CH₂NH₂?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 596 |
What is the common name for (CH₃)₃N?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 597 |
What type of amine is aniline (C₆H₅NH₂)?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 598 |
For the ammonolysis of alkyl halides to proceed efficiently via SN₂, the alkyl …
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 599 |
What is the product of the reduction of a nitrile (R-C≡N) with LiAlH₄?
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |
| 600 |
Reduction of nitroalkanes (R-NO₂) with Sn/HCl produces:
|
Fundamentals of Amines: Nomenclature, Isomerism, and Synthesis | View |