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ACS ORGANIC CHEMISTRY FINAL EXAM QUESTIONS AND ANSWERS - GRADED A+ | LATEST UPDATE 2026/2027 | VERIFIED.

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ACS ORGANIC CHEMISTRY FINAL EXAM QUESTIONS AND ANSWERS - GRADED A+ | LATEST UPDATE 2026/2027 | VERIFIED. In oxidative addition products of alkenes and alkynes, which reagents can be used? Cold, alkaline permanganate, osmium tetroxide and proxy acids. How are reductions of carbonyl compounds usually done? complex metal hydrides How are reductions of alkenes usually done? Catalytic hydrogenation How are reductions of alkynes usually done? Catalytic hydrogenation or alkali metals in ammonia (dissolving metal reductions) ACS ORGANIC CHEMISTRY FINAL EXAM 2025 What are the two types of free-radical reactions? substitution and addition. What is the IUPAC priority for naming? Carboxylic acid Ketone Aldehyde Alcohol In IUPAC naming, what is the suffix used for ketone groups? -one In IUPAC naming, what is the suffix used for alcohol groups? -nol In IUPAC naming, what is the suffix used for esters? -noate Benzyl group Phenyl group ethanoic acid (E) isomers vs. (Z) isomers. Which one is observed when the higher ranked molecules are on the same side? opposite? highest on same side: Z highest on opposite sides: E Electronwithdrawing groups are what type of directors? What is the one and only exception? Meta (deactivators) Halogens What can react with alcohols to produce a ketone? PCC (converts primary alcohols to aldehydes and secondary alcohols to ketones; doesn't affect C=C bonds. Chromic acid is an oxidizing reagent that does not oxidize ketones; but it can oxidize C-C double bonds. What can react with secondary alcohols to give ketones? KMnO4, NaOH. But it can also react with double bonds. ACS ORGANIC CHEMISTRY FINAL EXAM 2025 If the atom directly attached to the aromatic ring has lone pairs what type of director is it? what if it does not have lone pairs? lone pairs: activating, ortho, para director no lone pairs: deactivating, meta director If there is a NO2 group present, what IUPAC prefix will also be evident? nitro What is the predicted reaction? 1º alkyl halide with a strong base? weak base? poor nucleophile? strong base: Sn2 favored but E2 with strong non-nucleophilic bases weak base: Sn2 poor nucleophile: no reaction When are the terms ortho, meta, para used? when there are 2 substituents on the aromatic ring In IUPAC naming, what is NH2 on a phenyl ring referred to as? anilin Thank you for Purchasing this exam Study Guide. We provide high-quality academic materials to help students excel in exams. Our other Services include but not limited to: academic research, University & College assignments writing, essay writing, Online Classes, and research projects. Our services are reliable, affordable, and plagiarism-free. All the Best in your Exam. For more information; Contact us at: or 0R +254

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ACS ORGANIC CHEMISTRY FINAL EXAM
QUESTIONS AND ANSWERS - GRADED A+ | LATEST
UPDATE 2026/2027 | VERIFIED.



In oxidative addition products of alkenes and alkynes, which reagents can be used?

Cold, alkaline permanganate, osmium tetroxide and proxy acids.




How are reductions of carbonyl compounds usually done?

complex metal hydrides




How are reductions of alkenes usually done?
Catalytic hydrogenation




How are reductions of alkynes usually done?

Catalytic hydrogenation or alkali metals in ammonia (dissolving metal reductions)

,ACS ORGANIC CHEMISTRY FINAL EXAM 2025
What are the two types of free-radical reactions? substitution and
addition.




What is the IUPAC priority for naming?

Carboxylic acid > Ketone > Aldehyde > Alcohol




In IUPAC naming, what is the suffix used for ketone groups?

-one


In IUPAC naming, what is the suffix used for alcohol groups?

-nol




In IUPAC naming, what is the suffix used for esters?

-noate



Benzyl group



Phenyl group




ethanoic acid

,(E) isomers vs. (Z) isomers. Which one is observed when the higher ranked
molecules are on the same side? opposite?

highest on same side: Z highest
on opposite sides: E
Electronwithdrawing groups are
what type of directors? What is
the one and only exception?

Meta (deactivators)

Halogens




What can react with alcohols to produce a ketone?

PCC (converts primary alcohols to aldehydes and secondary alcohols to ketones;
doesn't affect C=C bonds.



Chromic acid is an oxidizing reagent that does not oxidize ketones;
but it can oxidize C-C double bonds.



What can react with secondary alcohols to give ketones?

KMnO4, NaOH. But it can also react with double bonds.

, ACS ORGANIC CHEMISTRY FINAL EXAM 2025




If the atom directly attached to the aromatic ring has lone pairs what type of
director is it? what if it does not have lone pairs?

lone pairs: activating, ortho, para director no lone

pairs: deactivating, meta director




If there is a NO2 group present, what IUPAC prefix will also be evident?

nitro



What is the predicted reaction? 1º alkyl halide with a strong base? weak base? poor
nucleophile? strong base: Sn2 favored but E2 with strong non-nucleophilic bases
weak base: Sn2 poor nucleophile: no reaction




When are the terms ortho, meta, para used?

when there are 2 substituents on the aromatic ring




In IUPAC naming, what is NH2 on a phenyl ring referred to as?

anilin

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