Functional Groups + Isomers Flashcards

1
Q

What is hybridization

A

Mixing of orbitals to create new ones
1. sp3
2. sp2

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2
Q

What is sp3 hybridization and why does it happen

A
  • One s orbital and three p orbitals hybridize to form four sp³ orbitals
  • Happens when an atom is surrounded by four groups of e- and single bonds ALKANES
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3
Q

What is sp2 hybridization and why does it happen

A
  • In sp2 orbitals only two of the p orbitals are hybridised, leaving one p orbital unaltered
  • So one p orbital remains with one e-
  • Takes place in carbon compounds containing double bonds ALKENES
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4
Q

Why do longer chains have higher boiling points

A

Because longer chains have more van der waals forces

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5
Q

What type of bond do saturated fats have

A

Only single bonds
Unsaturated fats have double bonds

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6
Q

How to create and name esters

A

Carboxylic acid + alcohol —> ester + water
Condensation reaction
Name: first word comes from alcohol, second from c.acid (ethyl propanoate)

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7
Q

What is an example of an ester bond

A

1 glycerol + 3 fatty acids —> triglyceride + 3 water
3 ester bonds

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8
Q

What are the types amines

A
  1. Primary
  2. Secondary
  3. Tertiary
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9
Q

What is the difference between amines and amides

A

Amines just have N but amides have N and C double bond O next to each other

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10
Q

How to make amides

A

Amine group and carboxyl group from 2 amino acids join creating water and a peptide bond

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11
Q

What is the purpose of phosphates and sulphydryls

A
  • Phosphates create phosphodiester bonds with carbon in pentose sugar backbone in DNA
  • Sulphydryls make disulphide bridges in amino acid chains creating the primary structure of a protein
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12
Q

What is are isomers

A

Molecules that have the same molecular formula but have different 3D structure

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13
Q

How can isomers differ

A
  1. Functional groups
  2. Carbon skeletons
  3. Different shapes
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14
Q

What are the different types of isomers

A
  1. Constitutional (structural) isomers
  2. Stereoisomers:
    - geometric (cis/trans) isomers
    - enantiomers (optical isomers)
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15
Q

Properties of enantiomers

A
  1. Has a chiral carbon
  2. Not superimposable
  3. A mixture containing both enantiomers is called a racemic mixture
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16
Q

What is a chiral carbon

A
  • A carbon that has four different groups attached to it
  • All enantiomers have a chiral carbon
17
Q

How to identify if a mixture is racemic

A

Shine plane-polarised light