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ACS Organic Chemistry II Final

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ACS Organic Chemistry II Final

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ACS Organic Chemistry
Course
ACS Organic Chemistry

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ACS ORGANIC CHEMISTRY II FINAL
2026 EXAMS, QUESTION AND
ANSWERS
What is the IUPAC priority for naming? - answerCarboxylic acid > Ketone > Aldehyde >
Alcohol

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

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

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

Benzyl group - answer

Phenyl group - answer

ethanoic acid - answer

(E) isomers vs. (Z) isomers. Which one is observed when the higher ranked molecules
are on the same side? opposite? - answerhighest on same side: Z
highest on opposite sides: E

Electron-withdrawing groups are what type of directors? What is the one and only
exception? - answerMeta (deactivators)
Halogens

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? - answerlone pairs: activating, ortho, para director
no lone pairs: deactivating, meta director

When are the terms ortho, meta, para used? - answerwhen there are 2 substituents on
the aromatic ring

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

Analine - answer

Amine - answer

Amide - answer

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

, What is the predicted reaction? 1º alkyl halide with a strong base? weak base? poor
nucleophile? - answerstrong 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? - answerstrong 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? - answerstrong 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)-1-
choloro-1-deuteriobutane? - answer(S)-1-deuterio-1-butanol (Sn2)

Where is the largest molecule on the periodic table? - answerBottom lefthand corner

Nucleophilic strength increase with increasing what? - answeratomic size

Which alkyl valid would you expect to undergo Sn1 hydrolysis most rapidly?
I, Br,Cl, or F? - answerI

In which reaction is a racemic mixture obtained?
In which reaction is an inversion of chirality obtained? - answerinversion: Sn2
racemic mix: Sn1

Cleavage of an ether usually requires a strong acid that has a conjugate base which is a
strong nucleophile, such as...? Depending on the type of alkyl group, the acid reaction
with the halide ion produces what? - answerHBr
HI
alkyl halide and an alcohol

When chirality rotates clockwise the chirality is... - answerR

When chirality rotates counterclockwise the chirality is... - answerS

A solution containing equal amounts of both enantiomers is called a..? - answerracemic
mixture

A meso compound contains multiple __________ centers but is nevertheless ________
because it possesses reflection symmetry - answerchirality

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Course
ACS Organic Chemistry

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