3.3.1 Introduction to organic chemistry Flashcards

1
Q

Define structural isomerism.

A
  • Same molecular formula but different structures
  • Chain isomerism (pentane, 2-methylbutane, 2,2,-dimethylpropane)
  • Position isomerism (1-bromopropane, 2-bromopropane)
  • Functional group isomerism (ethanol, hexene same MF but atoms arranged to give diff func. groups)
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2
Q

Define stereoisomerism.

A
  • Same structural formula but different spatial arrangement of atoms
  • Alkenes = E-Z isomerism.
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3
Q

How do E-Z isomerism arise?

A
  • restricted rotation around the C=C
  • 2 different groupsattached at both ends of double bond.
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4
Q

How do you name e-z isomerism?

A
  • determine the priority group on both sides of double bond.
  • Priority group = atom with the bigger atomic n.o.
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5
Q

What is Cahn-Ingold-Prelog priority rules?

A
  1. Compare atomic number of atoms directly attached to each side of double bond. Highest atomic number = priority.
  2. If atoms are the same, consider atoms at distance 2 from double bond.
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6
Q

What is the molecular formula?

A
  • The formula which shows the actual number of each type of atom
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7
Q
A
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8
Q

What is the empirical formula?

A

shows the simplest whole number ratio of atoms of each element in the compound

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9
Q

What is general formula?

A

algebraic formula for a homologous series e.g. CnH2n

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10
Q

What is structural formula?

A

shows the minimal detail that shows the arrangement of atoms in a molecule without shwoing bonds, eg for butane: CH3CH2CH2CH3

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11
Q

What is displayed formula?

A
  • show all the covalent bonds and atoms present in a molecule i.e.
    —H H
    H-C-C-H
    —H H
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