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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) What can react with alcohols to produce a ketone? ACS ORGANIC CHEMISTRY FINAL EXAM 2025 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. 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 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 What is the predicted reaction? 2º alkyl halide with a strong base? weak base? poor nucleophile? strong base: mostly E2 strong non-nucleophilic bases: mostly Sn2 poor nucleophile: Sn1/E2 (slow) in polar, protic solvents What is the predicted reaction? 3º alkyl halide with a strong base? weak base? poor nucleophile? strong base: E2 strong non-nucleophilic bases: Sn1/E1 in polar protic solvents poor nucleophile: Sn1/E1 in polar, protic solvents What is the configuration of the product in the base-catalyzed hydrolysis of (R)- 1choloro-1-deuteriobutane? (S)-1-deuterio-1-butanol (Sn2)

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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)




What can react with alcohols to produce a ketone?

,ACS ORGANIC CHEMISTRY FINAL EXAM 2025


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.




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 Electron-

withdrawing groups are what

type of directors? What is the

one and only exception?

Meta (deactivators)

Halogens

, 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




What is the predicted reaction? 2º alkyl halide with a strong base? weak base? poor
nucleophile?

strong base: mostly E2

strong non-nucleophilic bases: mostly Sn2

poor nucleophile: Sn1/E2 (slow) in polar, protic solvents




What is the predicted reaction? 3º alkyl halide with a strong base? weak base? poor
nucleophile? strong base: E2

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