11 Intro To Organic Chem Flashcards

1
Q

Hydrocarbons

A

Organic compounds which contain the elements carbon and hydrogen

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2
Q

Empirical formula

A

Simplest ratio of the number of atoms of the elements present in one molecule

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3
Q

Molecular formula

A

Actual number of atoms of the elements present in one molecule

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4
Q

Characteristics of a homologous series

A
  1. Same functional group
  2. Differs by a -CH2- group from one member to the next
  3. General formula
  4. Shows a gradual change in physical conditions
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5
Q

Alkane

A

C(n)H(2n+2)
Suffix: -ane
Prefix: alkyl-

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6
Q

Alkene

A

C(n)H(2n)
Suffix: -ene

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7
Q

Arene

A

Ar-R
Suffix: -benzene
Prefix: phenyl

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8
Q

Alkyl halide

A

R-X
Suffix: (nil)
Prefix: fluoro-/chloro-/

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9
Q

Aryl halide

A

Ar-X

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10
Q

Alcohol

A

R-OH
Suffix: -ol
Prefix: hydroxy-

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11
Q

Phenol

A

Ar-OH

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12
Q

Aldehyde

A

R/Ar -CH(O)
Suffix: -al
Prefix: oxo-

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13
Q

Ketone

A

Ar/R -(C=O)- Ar/R
Suffix: -one
Prefix: oxo-

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14
Q

Carboxylic acid

A

Ar/R-COOH
Suffix: -oic acid
Prefix: (nil)

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15
Q

Amide

A

Ar/R -CO(NH2)
Suffix: -amide
Prefix: (nil)

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16
Q

Amine

A

Ar/R -NH2
Suffix: -amine
Prefix: amino-

17
Q

Nitrile

A

Ar/R -C三N
Suffix: -nitrile
Prefix: cyano-

18
Q

Nitro compound

A

Ar/R -NO2
Suffix: (nil)
Prefix: nitro-

19
Q

Amino acids

A

C(COOH)(NH2)

20
Q

Ester

A

Ar/R -(C=O)O- Ar/R
Suffix: -oate
Prefix: (nil)

21
Q

Hybridisation

A

The mixing of atomic orbitals in various combinations to give a set of hybrid orbitals of equivalent energy for covalent bonding with other atoms

22
Q

sp^3 hybridisation

A

Mixing 1 s and 3 p valence orbitals
25.0% s character and 75.0% p character

23
Q

sp^2 hybridisation

A

Mixing 1 s and 2 p valence orbitals
33.3% s character and 66.7% p character

24
Q

sp hybridisation

A

Mixing 1 s and 1 p valence orbitals
50.0% s character and 50.0% p character

25
Q

7 types of chemical reactions

A
  1. Addition
  2. Substitution
  3. Elimination
  4. Condensation
  5. Hydrolysis
  6. Oxidation
  7. Reduction
26
Q

Nucleophile (Lewis base)

A

Electron pair donor and has a lone pair of electrons to be donated.
Can be negatively charged or neutral possessing a partial negative charge

27
Q

Electrophile (Lewis acid)

A

Electron pair accepter and is electron-deficient
Can be positively charged or neutral possessing a partial positive charge

28
Q

Homolytic fission

A

Each bonding atom takes 1 of the bonding electrons

29
Q

Heterolytic fission

A

One of the bonding atoms takes both bonding electrons

30
Q

Isomers

A

Same molecular formula but different arrangement of atoms in 3-dimensional space

31
Q

Constitutional isomers

A

Same molecular formula but different structural formula

32
Q

Chain isomers

A

Same functional group but different carbon chains

33
Q

Positional isomers

A

Same carbon chain but different position of functional group

34
Q

Functional group isomers

A

Differ in functional group

35
Q

Stereoisomerism

A

Same molecular and structural formula, but different spatial arrangement of their atoms

36
Q

Cis-trans isomers

A
  1. Restricted rotation about a covalent bond
  2. Two different groups/atoms attached to each carbon atom of that bond
    Cis: identical groups on same side
    Trans: identical groups on opposite sides
37
Q

Enantiomers

A

Stereoisomers with non-superimposable mirror images

38
Q

Chiral centres

A

Has 4 different groups (asymmetric)