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Organic Chemistry II ACS Final Exam Questions with Verified Answers | Latest 2024/2025 $11.49   Add to cart

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Organic Chemistry II ACS Final Exam Questions with Verified Answers | Latest 2024/2025

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  • Organic Chemistry II ACS
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  • Organic Chemistry II ACS

Organic Chemistry II ACS Final Exam Questions with Verified Answers | Latest 2024/2025

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  • August 9, 2024
  • 15
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • Organic Chemistry II ACS
  • Organic Chemistry II ACS
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Organic Chemistry II ACS Final Exam __., __., __., __., __., __.,




Questions with Verified Answers. __., __., __., __.,




When are the terms ortho, meta, para used?
__., __., __., __., __., __., __., __.,__., __., when there __., __.,



are 2 substituents on the aromatic ring
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What is the predicted reaction? 3º alkyl halide with a strong base
__., __., __., __., __., __., __., __., __., __., __.,



? weak base? poor nucleophile?
__., __., strong base: E2 __., __., __.,__., __., __., __.,




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



aniline __.,




If there is a NO2 group present, what IUPAC prefix will also be
__., __., __., __., __., __., __., __., __., __., __., __., __.



evident?
, nitro __.,__., __.,




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


(E) isomers vs. (Z) isomers. Which one is observed when the high
__., __., __., __., __., __., __., __., __., __., __.,



er 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


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
__., __., __., __., __.,




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
__., __., __.,

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