Exam 3 other info Flashcards

1
Q

E in german

A

entgegen, opposite

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2
Q

Z in german

A

zusammen, same

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3
Q

heat of hydrogenation

A

heat released during hydrogenation

allows us to ID stability

higher the heat of hydrogenation, the lower the alkene’s stability

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4
Q

why are more substituted alkenes more stable?

A

inductive effects and hyperconjugation

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5
Q

cycloalkenes with 5 C or fewer only…

A

exist in cis form

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6
Q

trans cyclo____ can be isolated and exists as enantiomers

A

octene

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7
Q

for trans cyclo—- and higher C number, cis is just as stable as trans

A

decene

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8
Q

Bredt’s rule

A

bicyclic compounds cannot have double bond at bridgehead unless one ring has 8 C or more

(if they do, they’re unstable)

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9
Q

Zaitsev’s rule

A

if more than one elimination product (alkene) is possible, the most substituted alkene is the major product

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10
Q

if you have to start an E2 rxn with a 1° halide…

A

use a bulky base

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11
Q

config. required for E2 to occur

A

anticoplanar

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12
Q

catalytic cracking

A

long chain alkane broken into a smaller alkane and an alkene

alkene is purified

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13
Q

dehydrogenation

A

removal of H2 from alkane to give alkene

requires a lot of energy

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14
Q

regioselectivity yields…

A

2+ constitutional isomers, with one being the major product

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15
Q

THF

A

tetrahydrofuran

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16
Q

2 types of halogenation

A

in anhydrous conditions - yields doubly halogenated product

in aqueous conditions - yields halohydrin (OH and X)

17
Q

hydrogenation requires…

A

heat, pressure

18
Q

catalysts used in hydrogenation

A

Pt, Pd, Ni

19
Q

heterogeneous catalysis

A

substrates in different phases

insoluble catalyst

fine particles of catalyst react with substrate to form products

20
Q

homogenous catalysis

A

catalyst is soluble

21
Q

4 types of information you can get from NMR

A
  1. # of signals – types of nuclei
  2. chemical shift – chemical environment
  3. area under signal – number of nuclei contributing
  4. splitting pattern – number of neighbors
22
Q

unit used to designate chemical shift

A

𝛅

23
Q

TMS

A

tetramethylsilane

reference compound

24
Q

moves signal downfield

A

deshielding

25
Q

multiplicity =

A

n + 1

26
Q

used to determine split peak height

A

Pascal triangle

27
Q

only — % of C is 13C

A

1.1%