Chapter Nine : Properties and reactions of organic compounds Flashcards

1
Q

Intermolecular forces

A

Dispersion
Dipole-Dipole
Hydrogen

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2
Q

Dispersion forces

A
Non-polar molecules
Electrons are momentarily distributed unevenly inducing a temporary dipole
Weak forces
Increase as chain length increases
Decreases with branching
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3
Q

Dipole-Dipole

A

Polar molecules
The partial positive charge on one attracts the partially negative charge on the other
Stronger than dispersion

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4
Q

Hydrogen bonding

A

Hydrogen bonds to FON

Stronger than dispersion and dipole-dipole

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5
Q

Structural isomers

A

Chain isomers - different branching in carbon chain
Positional isomers - different position of functional group
Functional isomers - Same atoms different functional groups

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6
Q

Stereoisomers

A

Cis isomers - when the groups are on the same side
Trans isomers - when groups are on opposite sides
Enantiomers - non-super imposable mirror images with a chiral centre

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7
Q

Alkane properties

A

Non-polar
As size increases dispersion forces increase, so MP and BP increases
As branching increases dispersion forces decrease and BP
Insoluble in water
Viscosity increases in size decreases as temp increases
Smaller ones have lower flashpoint

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8
Q

Flashpoint

A

Is the lowest temperature at which a liquid gives off enough vapour to start burning at its surface with the application of ignition source

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9
Q

Alkene/alkyne properties

A

Alkenes are more reactive than alkanes
Alkynes have low polarity
Highly flammable

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10
Q

Alcohol properties

A
Higher BP due to hydrogen bonding
BP increases as chain length increases
Smaller alcohols are soluble in water
Volatility decreases with length
Viscosity increases with length
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11
Q

Carboxylic acid properties

A

Smaller acids are soluble in water
Higher BP than alkanes/alcohols due to H bonds
Solubility decreases with chain length

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12
Q

Aldehydes and ketones properties

A

Volatile compounds
Solubility decreases with chain length
Higher BP than alkanes but lower than alcohols or acids

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13
Q

Ester properties

A

Lower BP than acids

Small esters are soluble in water

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14
Q

Amine properties

A

Weak base that accepts protons
Lower BP than alcohols
Solubility decreases with chain length

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15
Q

Amide properties

A

Have a higher BP/MP

Soluble but less soluble than amines/COOH

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16
Q

Reactions of alkanes

A

Combustion - reacts w O2 to for CO2,CO and H2O
Substitution - reacts with halogens in presence of UV light
Cracking - Using heat to break larger molecules to smaller molecules

17
Q

Reactions with alkenes

A

Combustion - reacts w O2 to for CO2, CO and H2O
Addition - double bond breaks when electronegative atom is reacted. H2 requires Pt, Pd or Ni catalyst
Forming alcohols - steam in presence of H3PO4 catalyst
Addition polymerisation - Adding monomers to make polymers

18
Q

Alcohol reactions

A

Combustion - reacts w O2 to form CO, CO2 and H2O
Substitution - Removing OH group and subbing it with a different functional group
Oxidation (1) - Oxidises to aldehyde then COOH in presence of H+/MnO4 or H+/Cr2O7-
Oxidation (2
) - oxidises to ketones in presence of H+/MnO4 or H+/Cr2O7-

19
Q

Haloalkanes reactions

A

Forming alcohols - reaction NaOH or KOH with haloalkane will give an alcohol

20
Q

Ester reactions

A

Condensation - Reaction between COOH and OH to form esters in presence of heat/sulfuric acid
Hydrolosis - When water is added to an ester to split it back into OH and COOH using heat and dilute acid

21
Q

Carboxylic acid reactions

A

Hydrolyse - seperate in water to become COO-

Acid-base - react with bases, Mg and metal carbonates

22
Q

COOH and amine reactions

A

Small amines act as base, COOH donates protons

COOH + NH2 > ammonium salt >(heat/dehydration) > amide + water