Organic 1 Section 3 - Unit 11: Introduction to Organic Chemistry Flashcards

1
Q

Define empirical formula

A

Simplest whole number ratio of atoms in a molecule

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2
Q

Define molecular formula

A

Actual ratio of the number of atoms in a molecule

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3
Q

Define displayed formula

A

Shows every atom and every bond in a molecule

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4
Q

Define structural formula

A

Shows arrangement of atoms in a molecule without showing every bond

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5
Q

Define structural isomer

A

Compounds with the same molecular formula but different structural formula

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6
Q

Define positional isomer

A

Compounds where the functional group is attached to the main chain at a different place

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7
Q

What is functional group isomerism

A

Same atoms but a different functional group due to a different arrangement of atoms

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8
Q

What is chain isomerism

A

Hydrocarbon chain is organised differently

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9
Q

Define stereoisomerism

A

When molecules have the same structural and molecular formula, but have a different arrangement of atoms in space

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10
Q

What is E-Z isomerism and how are the E and Z isomers decided?

A
  • E-Z isomerism is caused by the limited rotation about C=C double bonds
  • If the two substituents with the highest molecular mass are on the same side of the double bond, it is the Z isomer
  • If they are on different sides, it is the E isomer
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11
Q

State two general features of an homologous series of compounds (2 marks)

A
  • Same functional group

- Same general formula

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12
Q

How is the unpaired electron in a radical represented?

A

By a dot before or after the molecule

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13
Q

Define homolytic fission

A
  • The breakage of a bond to form 2 free radicals

- Each atom gets one electron from the covalent bond

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14
Q

Define free radical

A

A reactive species which possess an unpaired electron

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15
Q

Define heterolytic fission

A
  • The breakage of a bond to form ions

- One atom gets both electrons from the covalent bond

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16
Q

How is the formation of a covalent bond shown?

A

By a curly arrow that starts from a lone electron pair or from another covalent bond

17
Q

How is the breakage of a covalent bond shown?

A

By a curly arrow starting from the bond

18
Q

When do E-Z stereoisomers form? (2)

A
  • When there is restricted rotation around the C=C double bond.
  • When there are two different groups attached both ends of the double bond
19
Q

Explain the CIP rules used to determine the name of an alkene

A
  • Compare the atomic number of the atoms directly attached to each side of the double bond
  • The atom of higher atomic number is given priority