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What are intermolecular forces?
weaker than covalent bonds
the attraction between molecules
London dispersion, dipole dipole, H bonding
London Dispersion
temporary induced dipoles
the induced can induce other adjacent molecules
higher area contact = stronger LD = more E needed
Dipole - Dipole
stronger than LD forces
attraction b/w polar molecules
H-Bonding
strong DD attraction for H bonded to N,O,F with its lone pair
primary bonds are stronger in DD and HB
Noncovalent interactions (IM) affect properties and purification
boiling point
melting point
solubility
Melting point range
Distillation
Boiling point
depends on the strength of attractive forced b/w molecules
Strong forces = high BP = inc molec weight
branching lowers BP by dec area of contact
Melting point
Molec weight inc = inc melting point
influenced by packing of the crystal lattice
tight and organized packing requires more E to break it apart = higher melting point
impurities lowers the mp and broadens its range by disrupting the lattice = less E needed
odd carbon count = lower mp
Melting Point technique
pack dry powder in capillary tube
heat slowly towards its expected mp
record the first sign of melting and when its finished (this is the mp range)
Solubility
like dissolves like
polar solutes dissolve in polar solvents by HB, DD, Ion dipole
nonpolar solutes dissolve in nonpolar solvents by LD
Distillation
BP differences = IM differences
boiling liquids and collecting its vapor
high BP distills later
low BP distills first
Distillation - Ideal liquids and Raoult’s Law
IM are similar
obey the law to be ideal
Raoult’s Law
PA=(XA)(P0A)
PA = partial vapor pressure of A
XA = mole fraction of A in the liquid
PA∘ = vapor pressure of pure A
Simple Distillation
BP differs by a greater amount than 60 degrees
fewer theoretical plates
Fractional Distillation
BP differs by an amount less than 60 degrees
More theoretical plates = better separation
similar IM
Temp Composition Diagram
liquid comp curve = lower curve
vapor comp curve = higher curve
Vapor Pressure
Higher VP = lower BP
Azeotropes
boils at constant temp
vapor composition = liquid composition
cant be separated by distillation
Freq of IR
Freq: determined by bond strength and reduced mass
stronger bonds and lighter atoms = higher freq
High E = high freq = high wv# = shorter wavelength
Intensity of IR
Intensity: determined by change in dipole moment during vibration
Big dipole change = strong peak
small dipole change = weak peak
Stretches
change bond length along line of bond
strong and sharp
High E = High wv #
bend
doesn’t occur along bond length
weak and broad
low E = Low wv#
Aldehyde / ketone / C=O abs band
~1720 cm-1
OH abs band
~3600 - 3300 cm-1
broad
tongue shape
NH abs band
~3400 cm-1
sharp peak
primary = 2 peaks
secondary = 1 peak
tertiary = 0 peaks
Carboxy A abs band
~3200 - 2500 cm-1
broad, wide
mountain shape
C≡C
~2200 cm⁻¹
C≡N
~ 2250 cm⁻¹
C=C
~ 1650 cm⁻¹
C=N
~ 1650 cm⁻¹
sp CH
~3300 cm⁻¹
sp2 CH
~3150 - 3020 cm⁻¹
sp3 CH
~ 2950 cm⁻¹