4.2 Flashcards
Alcohols; properties
Polar O-H bond
London forces and H-bonds
Lower volatility than alkenes
Shorter chains soluble in water
Primary alcohol = ?
-OH attached to C with no C’s attached to it
Secondary alcohol = ?
-OH attached to C with 2 C’s attached to it
Tertiary alcohol = ?
-OH attached to C with three C’s attached to it
Alcohols; combustion
C2H5OH + 3O2 -> 2CO2 + 3H2O
Primary alcohol; distillation and reflux
Distillation of primary = ALDEHYDE
Reflux of primary = CARBOXYLIC ACID
Secondary alcohol; reflux
Reflux of secondary = ketone
Conditions for distillation and reflux
Acidified potassium dichromate
K2Cr2O7/H2SO4
definition of NUCLEOPHILE
Species that donates a lone pair of electrons
Haloalkanes; Nucleophilic substitution
Nucleophile e.g. OH- attacks carbon making C slightly +ve and (e.g.) Cl slightly -ve
Nucleophile suns out the halide
Highest rate of hydrolysis = 1-iodo…
Slowest rate of hydrolysis = 1-chloro…
CFCs
i) CF2Cl2 -> CF2Cl• + Cl•
p1) Cl• + O3 -> ClO• + O2
p2) ClO• + O-> Cl• + O2
Overall) O3 + O -> 2O2
Mass spectrometry
Loses an e- to form +ve ion = molecular ion
Detects mass to charge ratio m/z
e.g. CH3CH2CH2OH -> CH3CH2CH2OH+ + e-
Molecular ion peak=clear peak at highest m/z value (usually small)
Fragmentation (mass spec)
e.g. CH3CH2CH2OH+ -> CH2OH+ + CH3CH2•
Fragment ion and RADICAL formed
Infrared spectroscopy
Covalent bonds absorb IR radiation = bend/stretch more (distance/angle changes)
Heavier=slower
Stronger bond=faster