Introduction to Organic Chemistry Flashcards

1
Q

Define molecular formula

A

the actual number of atoms of each element in a molecule

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2
Q

Define empirical formula

A

simplest ratio of atoms of each element in a compound

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3
Q

Define general formula

A

number of atoms of each element in a substance which has n carbon atoms

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4
Q

Define structural formula

A

this shows the arrangement of atoms in a molecule without showing every bond

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5
Q

Define displayed formula

A

this shows all the bonds and atoms in a molecule

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6
Q

Define skeletal formula

A

this uses lines to represent bonds, each point represents a carbon and hydrogen atoms aren’t shown

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7
Q

What is a hydrocarbon

A

a compound that contains only carbon and hydrogen

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8
Q

What are saturated hydrocarbons

A
  • contain single carbon-carbon bonds
  • alkanes
  • general formula CnH2n+2
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9
Q

What are unsaturated hydrocarbons

A
  • at least one multiple bond between carbon atoms
  • alkenes (double bond)
  • alkynes (triple bond)
  • general formula CnH2n
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10
Q

What is a homologous series

A

a family of compounds containing the same functional group but with each successive member of the series differing by a CH2 group

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11
Q

What are the trends in homologous series

A
  • trends in physical properties
  • an increase in CH2 group is an increase of Mr by 14
  • melting and boiling points increase as the chain length increases
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12
Q

What is a functional group

A

an atom/group responsible for the characteristic reactions of the compound

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13
Q

What is an aromatic compound

A

compounds containing a benzene ring, they are unsaturated hydrocarbons and have the formula C6H6

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14
Q

What are the IUPAC rules for nomenclature

A
  • find the longest C chain
  • give the alkyl group the lowest number
  • list alkyl groups alphabetically
  • double bond/halogens have priority over alkyl groups
  • constants cant be next to constant so add ‘a’
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15
Q

What homologous series have their functional group always at the end

A
  1. carboxylic acids (-oic)
  2. aldehydes (-al)
  3. nitriles (-nitrile)
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16
Q

Define structural isomerism

A

molecules with the same molecular formula but a different structural formula

17
Q

What is chain isomerism

A

carbon chain is arranged differently

18
Q

What is positional isomerism

A

position of functional group changes

19
Q

What is functional group isomerism

A

same atoms but a different functional group

20
Q

What is stereoisomerism

A

when molecules have the same structural formula but have a different arrangement of atoms in space

21
Q

When does E/Z stereoisomerism occur

A

it is caused by the limited rotation about the C=C double bonds

criteria for a compound:
- must have a C=C double bond
- each carbon of the C=C must have 2 different groups attached to it

22
Q

How are E and Z isomers decided

A
  • if the groups of higher priority are on the same side of the double bond it is Z ISOMERISM
  • if the groups of higher priority are on diagonally opposite sides of the double bond it is E ISOMERISM
23
Q

Explain how the Cahn-Ingold-Prelog (CIP) priority rules can be used to deduce which isomer it is

A
  1. look at the atoms attached directly to the carbon atoms and decide which of the 2 atoms has the highest priority
  2. if the 2 atoms attached to a carbon atom are the SAME, then you will need to find the first point of difference - the group with the higher atomic number at the first difference is given higher priority