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ACS Organic Chemistry Final Exam Study Guide with complete solutions |Latest 2024/2025 $11.49   Add to cart

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ACS Organic Chemistry Final Exam Study Guide with complete solutions |Latest 2024/2025

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  • Course
  • ACS Organic Chemistry
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  • ACS Organic Chemistry

ACS Organic Chemistry Final Exam Study Guide with complete solutions |Latest 2024/2025

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  • August 9, 2024
  • 16
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • ACS Organic Chemistry
  • ACS Organic Chemistry
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ACS Organic Chemistry Final Exam
__., __., __., __., __.,




Study Guide with complete solutions. __., __., __., __., __.,




What is the equation for Huckel's numbers? What are Huckel's numbers?
__., __., __., __., __., __., __., __., __., __., __.,_


_., 4n + 2 __.,__.,__.,__.,__., __., __.,




Huckel's numbers are the number of electrons in a pi system in aromatic
__., __., __., __., __., __., __., __., __., __., __., __., __.


compounds
,




Do lone pairs contribute to hybridization?
__., __., __., __., __., __.,__., Yes
__.,




How do you draw a Lewis structure?
__., __., Determine the number of
__., __., __., __., __.,__., __., __., __., __., __.,


valence electrons for each atom and add them up
__., __., __., __., __., __., __., __.,




Attempt to form octets at each atom, counting bonds as two electrons
__., __., __., __., __., __., __., __., __., __., __.,




How is free energy related to acidity?
__., __., In a reaction where a proton
__., __., __., __., __.,__., __., __., __., __., __., __., __


is lost, decreasing free energy implies more stability in the products, and
., __., __., __., __., __., __., __., __., __., __., __., __.


thus more willingness to donate a proton, meaning more acidic.
, __., __., __., __., __., __., __., __., __.,




What is the Gibbs free energy equation for an acid reaction?
__., __., __., __., __., __., __., __., __., __., __.,__., __., Delta __.,


G = -RTln([A-][H3O+]/[HA][H2O])
__., __.,




What are the factors influencing acidity?
__., __., __., __., __., __.,__., __., MARIO minus M __., __.,




How do polar protic solvents affect SN1, SN2, E1 and E2 reactions?
__., __., __., __., __., __., __., __., __., __., __., __.,__., __.,


Polar protic solvents stabilize the carbocations intermediate in SN1 and E1
__., __., __., __., __., __., __., __., __., __., _

, reactions, and they do not hinder E2 reactions, but they will block the
_., __., __., __., __., __., __., __., __., __., __., __., __., __.,


stereocenter/alpha carbon in SN2 reactions. __., __., __., __.,




How does size of a molecule affect nucleophilicity in polar protic vs
__., __., __., __., __., __., __., __., __., __., __., __.,



polar aprotic solvents?__.,Larger size in polar protic —
__., __.,__., __., __., __., __., __., __.,


> greater nucleophilicity
__., __.,




Smaller size in polar aprotic —> greater nucleophilicity
__., __., __., __., __., __., __.,




Do non- __.,


polar solvents favor unimolecular or bimolecular mechanisms in substitutio
__., __., __., __., __., __., __., __.,



n elimination reactions?
__., Bimolecular, because the charged leaving
__., __.,__., __., __., __., __., __., __.,


group does not want to leave into a non-polar environment
__., __., __., __., __., __., __., __., __.,




-al __.,




-ol or hydroxy-
__., __.,




-one
-oic acid __.,




-oate __.,




-ether or alkoxy- __., __.,




Iodo- or Bromo- etc. __., __., __., __.,




-amide

Amino- or -amine __., __., __.,__., __.,Aldehyde
Alcohol
Ketone

, Carboxylic acid __.,




Ester
Ether
Alkyl halides __.,




Amide
Amine


Constitutional Isomer A compound with the same atoms but differen
__., __.,__., __., __., __., __., __., __., __., __.,


t atoms bonded to each other
__., __., __., __., __.,




Stereoisomers __.,__., __.,Molecules with the same atoms differing only in 3D
__., __., __., __., __., __., __., __., __.


configuration
,




Enantiomers Stereoisomers with exactly opposite stereochemical
__.,__., __., __., __., __., __., __.


designations at all stereogenic carbons
, __., __., __., __.,




Diasteriomers Stereoisomers with several changes in the
__.,__., __., __., __., __., __., __., __.,


stereochemical designations of stereogenic carbons (not completely
__., __., __., __., __., __., __.,


opposite)


R __.,__., __., Clockwise


S __.,__., Counterclockwise
__.,




cis __.,__., Same
__.,

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