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ACS Organic Chemistry II Final Exam Questions & Answers Grade A+

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ACS Organic Chemistry II Final Exam Questions & Answers Grade A+

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ACS Organic Chemistry II Final Exam
Questions12

What is the IUPAC priority for naming? - ANSWERSCarboxylic acid > Ketone > Aldehyde >
Alcohol



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



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



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



Benzyl group - ANSWERS



Phenyl group - ANSWERS



ethanoic acid - ANSWERS



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

highest on opposite sides: E



Electron-withdrawing groups are what type of directors? What is the one and only exception? -
ANSWERSMeta (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? - ANSWERSlone pairs: activating, ortho, para director

no lone pairs: deactivating, meta director



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



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



Analine - ANSWERS



Amine - ANSWERS



Amide - ANSWERS



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



What is the predicted reaction? 1º alkyl halide with a strong base? weak base? poor
nucleophile? - ANSWERSstrong 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? - ANSWERSstrong base: mostly E2

strong non-nucleophilic bases: mostly Sn2

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

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