MD - Organic Functional Groups and Reactions Flashcards

1
Q

For the group -COOH, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Carboxylic acid
ii) Carboxy-
iii) -oic acid
iv) Ethanoic acid

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2
Q

For the group -COCl, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Acyl chloride
ii) N/a
iii) -oyl chloride
iv) Ethanoyl chloride

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3
Q

For the group -CO-CO-, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Acid anhydride
ii) N/a
iii) -oic anhydride
iv) Ethanoic anhydride

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4
Q

For the group -COO-, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Ester
ii) N/a
iii) -oate
iv) Ethyl methanoate

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5
Q

For the group -CO-, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Ketones
ii) N/a
iii) -one
iv) Propanone

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6
Q

For the group -OH, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Alcohol (hydroxide)
ii) hydroxy-
iii) -ol
iv) Propanol

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7
Q

For the group -NH₂, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Primary amine
ii) amino-
iii) -amine
iv) Methylamine

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8
Q

For the group -NH, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Secondary amine
ii) N/a
iii) -amine
iv) aminomethane

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9
Q

For the group -N–, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Tertiary amine
ii) N/a
iii) -amine
iv) Trimethylamine

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10
Q

For the group -NO₂, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Nitro
ii) Nitro-
iii) N/a
iv) Nitrobenzene

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11
Q

For the group -C₆H₅, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) Phenyl
ii) phenyl-
iii) -benzene
iv) aminobenzene

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12
Q

For the group -C=C-, give:

i) The group name
ii) Its prefix in a compound
iii) Its suffix in a compound
iv) An example of a molecule it can be found in

A

i) alkene
ii) N/a
iii) -ene
iv) Butene

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13
Q

State how you would classify and name an organic compound

A

1) The main functional group is used as the suffix and the other functional groups are added as prefixes
2) The order of importance is used to show the main functional group; where Carboxylic acids are the most important, and phenyl groups are least
3) If you need to include more than one functional group prefix, then list them in alphabetical order

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14
Q

Name the 7 types of organic reactions

A

1) Addition
2) Elimination
3) Substitution
4) Condensation
5) Hydrolysis
6) Oxidation
7) Reduction

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15
Q

Describe, and state the functional groups which undergo addition reactions

A
  • Description: 2 molecules join together to form a single product, which involves breaking a double bond
  • Functional groups: Alkenes, Aldehydes & Ketones
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16
Q

Describe, and state the functional groups which undergo elimination reactions

A
  • Description: Involves removing a functional group which is released as part of a small molecule - often a double bond is formed
  • Functional groups: Halogens and Alcohols
17
Q

Describe, and state the functional groups which undergo substitution reactions

A
  • Description: A functional group on a molecule is swapped for a new one
  • Functional groups: Halogens, Alcohols & Arenes
18
Q

Describe, and state the functional groups which undergo condensation reactions

A
  • Description: 2 molecules get joined together with the loss of a small molecule (e.g. water) - the opposite of hydrolysis
  • Functional groups: Carboxylic acids, Acyl Chlorides & Amides
19
Q

Describe, and state the functional groups which undergo Hydrolysis

A
  • Description: Water is used to split apart a molecule creating 2 smaller ones - the opposite of condensation
  • Functional groups: Esters, Polyesters, Polyamides & Acid Anhydrides
20
Q

Describe, and state the functional groups which undergo Oxidation reactions

A
  • Description: The loss of electrons, Hydrogen atoms or the gain of an Oxygen atom
  • Functional groups:
    Alcohol → Aldehyde → Carboxylic Acids
21
Q

Describe, and state the functional groups which undergo Reduction reactions

A
  • Description: The gain of electrons, Hydrogen atoms or the loss of an Oxygen atom
  • Functional groups:
    Carboxylic Acid → Aldehyde → Alcohol
22
Q

Name 6 chemical species

A

1) Radical
2) Electrophile
3) Nucleophile
4) Carbocation
5) Saturated Molecule
6) Unsaturated Molecule

23
Q

Define Radical

A

An atom, molecule or ion that has an unpaired electron

24
Q

Define Electrophile

A

Attracted to molecules with areas of high electron density where it accepts electrons

25
Q

Define Nucleophile

A

Attracted to regions of positive charge density (e.g. δ+ C atoms in molecules with polar bonds)
It can donate a pair of electrons to form a dative covalent bond (so it must have a lone pair)

26
Q

Define Carbocation

A

An organic ion with a positively charged carbon atom. They form when a bond breaks and the electrons move away from the carbon atom

27
Q

Define Saturated Molecule

A

All the C-C bonds are single

28
Q

Define Unsaturated Molecule

A

There is at least one C=C double bond

29
Q

State the 5 different organic mechanisms

A

1) Radical substitution
2) Electrophilic addition
3) Nucleophilic substitution
4) Electrophilic substitution
5) Nucleophilic addition

30
Q

State the 3 stages of Radical substitution

A

1) Initiation
2) Propagation
3) Termination

31
Q

Describe electrophilic addition

A

The δ+ of a polar molecule or positive ion (electrophile) is attracted to the electrons in a double bond. The bond opens up and the molecule or ion is added

32
Q

Describe nucleophilic substitution

A

The δ- of a polar molecule or a negative ion (nucleophile) is attracted to the δ+ of a polar bond in a molecule. The nucleophile replaces an atom or group in the molecule

33
Q

Describe electrophilic substitution

A

The δ+ of a polar molecule or a positive ion (electrophile) is attracted to an electron rich region (usually to aromatic compounds) and is substituted for an existing group

34
Q

Describe nucleophilic addition

A

The δ- of a polar molecule or a negative ion (nucleophile) is attracted to the δ+ of a polar double bond. The bond opens up and the nucleophile is added