Week 9 - Organic Chemistry I Flashcards

1
Q

Primary, Secondary, Tertiary, Quaternary carbon

A

a carbon that is bonded with 1, 2, 3, and 4 other carbons

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2
Q

Single bond

A

AKA saturated, meaning ‘full’

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3
Q

Double and triple bonds are…

A

unsaturated

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4
Q

Heteroatoms

A

PONS: phosphorus, oxygen, nitrogen, sulfur (and halides)

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5
Q

Hydrocarbon suffixes

A

single bonds: -ane
double bonds: -ene
triple bonds: -yne

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6
Q

Cyclic hydrocarbons

A

single bonds: cycloalkane
double bond: cycloalkene
3 double/3 single: aromatics, benzene rings

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7
Q

10 base names (alkane)

A

methane
ethane
propane
butane
pentane
hexane
heptane
octane
nonane
decane

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8
Q

gases vs. liquids

A

meth - but: gases
pent - dec: liquids

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9
Q

Hydrocarbons are…

A

non-polar

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10
Q

the only intermolecular force present in hydrocarbons is…

A

London Dispersion Forces

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11
Q

as molar mass increases, alkanes become…

A

less volatile

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12
Q

shape of cyclopropane, cyclobutane, cyclopentane?

A

triangle, square, pentagon

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13
Q

C to H ratio in alkanes

A

C(n) H(2n+2)

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14
Q

C to H ratio in alkenes

A

C(n) H(2n)

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15
Q

ethene –> octene

A

boiling point increases

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16
Q

C to H ratio in alkynes

A

C(n) H(2n-2)

17
Q

How to calculate degree of unsaturation?

A

(Difference in # of hydrogens for the saturated version vs alkane version) / 2; so for example octyne has 14 H, octane has 18, so 4/2 =2 and octyne has 2 units of unsaturation

18
Q

How many units of unsaturation for each bond?

A

double bond - 1
triple - 2
each ring - 1
can use this when calculating for more complex molecules by just counting how many of each thing there is

19
Q

Most common alkyl substituents

A

methyl, ethyl, propyl, butyl, chloro (Cl), bromo (Br), iodo (I), fluoro (F)

20
Q

subsituents go in…

A

alphabetical order (prefixes like di, tri are ignored)

21
Q

Naming order in cycloalkanes

A

if only one substituent, no need to specify number
if multiple, try to make it so they have the lowest number possible and they are in increasing number and alphabetical order
also try to get the fewest sum of all numbers possible

22
Q

Cyclo ALWAYS…

A

gets the base name

23
Q

in cycloalkenes…

A

carbons of the double bond are assigned number 1 and 2

24
Q

naming alkenes

A

longest chain must include the double bond, start numbering from the end closest to the double bond

25
Q

naming alkynes

A

longest chain must include the triple bond, start numbering from the end closest to triple bond

26
Q

if both double and triple bonds are present…

A

number the chain to get the lowest possible numbers; if a tie, -ene gets the lowest numbers

27
Q

Benzene ring hybridization

A

all ring carbon atoms sp2

28
Q

organic compounds that are not aromatic (benzene) are…

A

aliphatic

29
Q

aromatic (benzene) rings have special…

A

stability (low reactivity)

30
Q

Naming on benzene rings

A

substituent on location 1, then anything else is ortho, then meta, para

31
Q

Alkynes will always be drawn (hybridization)…

A

as a straight line, because they are sp