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Properties of Organic chem
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Alkane - states of matter
C1 to C4 are GASES, C5 to C15 are LIQUID, rest are SOLIDS
Alkane - Boiling point (straight & branch chain)
Boiling point of straight chain alkanes increases with increasing size of m/c
Due to no. of e ⬆, strength of ID-ID forces ⬆
Boiling point of branching alkanes decrease while increasing branching
Due to m/c having less SA, strength of ID-ID forces ⬇
Alkane - Reactivity
Unreactive
are non-polar
unreactive towards polar or ionic reagents
not attacked by nucleophiles or electrophiles
reacts only with non-polar reagents under UV light or heat
Alkenes - Reactivity
More reactive than alkanes
Pi bond is weaker than sigma bond.
Double bond is rich in e-, hence attacked by electrophiles
Halogenoalkanes - Reactivity
R -- I > R – Br > R – Cl
Reactivity decrease due to ⬇bond length, ⬇bond energy, bond strength ⬆
C – F bond too strong, it is unreactive
Alcohol - Volatility
< 12 carbon atoms → Liquid at RT
Bp of Alcohol is higher than ethers of similar Mr due to strong H-B
Alcohol - Solubility
Solubility ⬇ as no. of carbon increases, long carbon chain less polar
Lower alcohols are soluble due to OH group that can form H-B w water
Carbonyl Compounds
Aldehydes more reactive than ketones
Size of alkyl ⬆
Steraic hindrance ⬆
Reactivity ⬇
Carboxylic acid - Boiling point
Relatively higher due to H – O
Higher than alcohol of similar Mr
Due to presence of highly electro-ve
Atoms in C=O & O – H bond become more polar
Which forms a stronger H – Bond
Carboxylic acid - Solubility
decreases as length of carbon chain increase, m/c becomes less polar
Methanoic acid & ethanoic acid completely soluble
Benzoic acid is soluble in hot water & crystallizes when cooled
Ester - Physical properties
Same mlc formula as carbo acids
Neutral
Lower bp than carbo acids ( ❌H-bond)
Mostly insoluble in water, but small esters are fairly soluble as chain length is short (more polar)
Strong fruity smell
Smallest ester will have minimum 2 carbons (draw it out, it make sense)