Structure and nomenclature of organic compounds Flashcards

1
Q

-O-H

A

alcohol (ol)

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2
Q
  • C=O

- H

A

Aldehyde (al)

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3
Q

> C=O

A

carbonyl (ketone) (one)

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4
Q

COOH

A

carboxyl (carboxylic acid) (oic acid)

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5
Q

=O

  • C
    • O-
A

ester (alkyl alkanoate)

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6
Q

-O-

A

ether (alkoxyalkane, or name the two groups attached to the ether link)

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7
Q

-NH2

A

amiNe (amine)

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8
Q

-CONH2

A

amiDe (amide)

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9
Q
  • Cl
  • Br
  • I
A

haloalkanes (cholro)
(bromo)
(iodo)

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10
Q

Addition of primary alcohols

A

oxidisation–> carboxylic acids and aldehydes

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11
Q

adition of secondary alcohols

A

oxidisation–> aldehydes

acids cannot be made as the -OH is not at the end of the chain

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12
Q

What does substitution require?

A

A catalyst of sorts: UV light (easier to control), or heat.

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13
Q

alcohol + H+ + Cr2O72- (catalyst)

A

oxidisation: aldehyde

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14
Q

aldehyde + H+ + Cr2O72- (catalyst)

A

oxidisation: carboxylic acid

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15
Q

alcohol + NH3 + alumina(catalyst) + high temp

A

substitution: amine

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16
Q

alcohol + (al2O3) + high temp

A

dehydration: alkene

17
Q

carboxyl acid + base

A

acid/base neutalisation: ;)

18
Q

carboxyl acid + water

A

still acid/base: dissociation eg: CH3COO- + H3O+

19
Q

carbon valence, and what this means?

A

4 electrons. Therefore carbon can form four single bonds or multiple bonds to complete the outer sheel

20
Q

unsaturated hydrocarbons

A

single bonds

21
Q

saturated hydrocarbons

A

double and triple

22
Q

cyclic hydrocarbons

A

different combinations of double and single bonds b/w each carbon atom.

23
Q

benzene formula

A

C6H6

24
Q

structual isomers

A

the basic shit. they have similar properties.

25
Q

stereoisomers: optical isomers

A
  • have chiral centre
  • mirror image is not superimposable.
  • eg hand
  • enantiomers
26
Q

stereoisomers: geometric isomers

A
  • cis and trans
  • cis= same side
  • trans= oppisite
  • have diff chemical and physical properties
27
Q

primary alcohol

A

terminal

28
Q

seconday alcohol

A

the carbon the OH is attached to is bonded to 2 other carbons.

29
Q

Tertiary alcohol

A

the carbon that the OH group is attached to is bonded to 3 other carbons