Final Exam Flashcards

extra things to remember (31 cards)

1
Q

enthalpy

A

heat energy exchange between rxn and surroundings

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2
Q

bonds broken

A

energy needed (input)

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3
Q

bonds formed

A

energy released (output)

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4
Q

change in enthalpy

A

(BDE bonds broken)-(BDE bonds formed)

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5
Q

exothermic stability

A

bonds formed more stable

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6
Q

endothermic stability

A

bonds broken more stable

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7
Q

entropy

A

moleculur disorder, randomness, freedom
* change in S

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8
Q

positive change in G

A

not spontaneous and exergonic

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9
Q

negative change in G

A

spontaneous and endergonic

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10
Q

where do you look for change in G

A

line between reactants and products

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11
Q

what do you look at for activation energy

A

line from reactants to peak

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12
Q

what is change in G when it’s product favored

A

△G<0
more products

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13
Q

when keq=0.25, is it product or reactant favored

A

reactant

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14
Q

when keq=2, is it product or reactant favored

A

product

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15
Q

what to kinetic products favor

A

lower activation energy

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16
Q

what do thermodynamic products favor

17
Q

transition state for exothermic vs endothermic rxn

A

exothermic rxn - early transition state
endothermix rxn - later transition state

18
Q

nucleophile

A

donate electrons

19
Q

electrophiles

A

accept electrons

20
Q

proton transfer

A

arrow goes from electrons on base to H of acid and then from the H-atom bond to the atom

21
Q

what does rearrangment occur

A
  • go from primary to seconary ot tertiary
  • secondary to tertiary
  • tertiary to tertiary w/ resonance
22
Q

carbocation stability

A

3 - most stable
1- least stable

23
Q

naming alkyl halides
F, Cl, I, Br

A

fluoro
chloro
iodo
bromo

24
Q

naming rule

A
  • Give the lowest possible number to the substituent (regardless of its priority)
  • if tie, then do alphabetical
  • if 1 chiral center, don’t have to put number in front of R/S; number after
    (R/S)-X-substituent
    ex. (R)-5-chloro
  • if more than one chircal center, number before R/S, no number after ex. (3R, 4S) - dichloro
    (XR, XS)-di/tri-substitueint
25
to determine major vs minor products
1. determine if base is bulky or small - bulky: major product = less substitued alkene - small: major product = more substitued
26
what does subsituted mean
how many substituents are on the alkene
27
e2
look for all beta hydrogens alkene formed
28
when a primary is reacted under slovolysis, what product is formed
only product from the rearrangment is formed
29
major product for E1 rxn always
more subsituted one, zaitsev
30
NaOH
Na is a spectator ion so OH gets attached
31
halohydrogenation
redraw alkene without pi bond, figure out where H goes then draw + on opposite side of alkene from H, then nuc. attack