IB Chemistry HL Topic 10 & 20

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33 Terms

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homologous series

- successive members of a homologous series differ by a -CH2 group
- members of HS can be represented by same general formula
- members of homologous show a gradation in their physical properties
- members of a series have similar chemical properties

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functional group

small group of atoms attached to a carbon atom in a molecule, giving characteristic properties to the compound

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chemical properties

illustrated by sections that follow on different homologous series

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physical properties

result of changes that occur in the strength of Van der Waals' forces w/ increasing molar mass and in some cases a change in molecular polarity

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condensed structural formula

bonds are omitted, side chains put in brackets and repeated identical groups collected together

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molecular formula

gives actual number of each type of atom in molecule

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empirical formula

simplest whole number ratio

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isomer

different compounds that have the same molecular formula

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structural isomer

atoms joined in different order so that they have different structural formulae

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stereo isomer

order the atoms are joined together is the same, but the molecules have a different arrangement of atoms in space and hence different 3D shapes

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alkane

IPUAC name: -ane
- low chemical reactivity
- substitution: halogenation

<p>IPUAC name: -ane<br>- low chemical reactivity<br>- substitution: halogenation</p>
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alkene

IUPAC name: -ene

<p>IUPAC name: -ene</p>
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alcohol

IUPAC name: -anol

<p>IUPAC name: -anol</p>
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amine

IUPAC name: -anamine

<p>IUPAC name: -anamine</p>
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aldehyde

IUPAC name: -anal

<p>IUPAC name: -anal</p>
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ketone

IUPAC name: -anone

<p>IUPAC name: -anone</p>
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carboxylic acid

IUPAC name: -anoic acid

<p>IUPAC name: -anoic acid</p>
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amide

IUPAC name: -anamide

<p>IUPAC name: -anamide</p>
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ester

IUPAC name: -anoate

<p>IUPAC name: -anoate</p>
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nitrile

IUPAC name: -anenitrile

<p>IUPAC name: -anenitrile</p>
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saturated reactant

compounds which only contain single bonds

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unsaturated reactant

compounds which contain double or triple bonds

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electrophile

- electron-deficient species which is attracted to parts of molecules which are electron rich
- positive ions or have partial positive charge

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nucleophile

- electron-rich species which is attracted to parts of molecules which are electron deficient
- nucleophilies have a lone pair of electrons and may also have a negative charge

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combustion reaction

Complete combustion: C8H18 + O2 --> CO2 + H2O
Incomplete combustion: C8H18 + O2 --> CO + H2O + C + CO2
- these products w/ other minor products of hydrocarbon combustion and residue of lead compounds, are major sources of air pollution

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addition reaction

- occurs when 2 reactants combine to form a single product
- characteristic of unsaturated compounds
- (i.e. C2H4 + Br2 --> C2H4Br2)

<p>- occurs when 2 reactants combine to form a single product<br>- characteristic of unsaturated compounds<br>- (i.e. C2H4 + Br2 --&gt; C2H4Br2)</p>
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halogenation reaction

- occurs when one atom or group of atoms in a compound is replaced by a different atom or group
- characteristic of saturated compounds and aromatic compounds
- (i.e. CH4 + Cl2 --> CH3Cl + HCl)
- initiation, propagation, termination

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elimination reaction

- occurs when a small molecule is lost from a larger compound
- usually results in the formation of a double or triple bond
- when H2O is the eliminated molecule -- reaction is dehydration
- (i.e. C2H5OH --> C2H4 +H2O)

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addition-elimination reaction

- occurs when two reactants join together and in the process a small molecule is lost
- reaction occurs b/w a functional group in each reactant
- also known as -- condensation reaction
- (i.e. RNH2 + R'COOH --> R'COHNR + H2O)

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nucleophilic substitution reaction (SN2)

- Primary halogenoalkanes: SN2 mechanism
--> one-step mechanism dependent on concentration of both halogenoalkane and hydroxide ion

<p>- Primary halogenoalkanes: SN2 mechanism<br>--&gt; one-step mechanism dependent on concentration of both halogenoalkane and hydroxide ion</p>
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nucleophilic substitution reaction (SN1)

- Tertiary halogenoalkanes: SN1 mechanism
--> two-step mechanism
--> 1st step: halogenoalkane ionizing by breaking its carbon-halogen bond heterolytically
--> 2nd step: carbocation intermediate is attacked by nucleophilie to form new bond

<p>- Tertiary halogenoalkanes: SN1 mechanism<br>--&gt; two-step mechanism<br>--&gt; 1st step: halogenoalkane ionizing by breaking its carbon-halogen bond heterolytically<br>--&gt; 2nd step: carbocation intermediate is attacked by nucleophilie to form new bond</p>
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homolytic fission

when covalent bond breaks by splitting the shared pair of electrons b/w two products
- produces two free radical each w/ unpaired electron

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heterolytic fission

- when a covalent bond breaks with both the shared electrons going to one of the products
- produces two oppositely charged ions