formulas Flashcards

1
Q

Relationship between frequency and wavelength

A

v=c/ƛ

where v=frequency (Hz) c=speed of light (3x10^8ms^-1) and ƛ=wavelength (nm)

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2
Q

Relationship between frequency and energy

A

E=hv

where E=energy (J) h=Planck’s constant (6.626x10^-34 Js) v=frequency

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3
Q

Factor of a metre: femto (f)

A

10^-15

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4
Q

Factor of a metre: pico (p)

A

10^-12

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5
Q

Factor of a metre: nano (n)

A

10^-9

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6
Q

Factor of a metre: micro (µ)

A

10^-6

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7
Q

Factor of a metre: milli (m)

A

10^-3

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8
Q

Factor of a metre: centi (c)

A

10^-2

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9
Q

Factor of a metre: deci (d)

A

10^-1

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10
Q

Factor of a metre: kilo (k)

A

10^3

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11
Q

Factor of a metre: mega (M)

A

10^6

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12
Q

Factor of a metre: giga (G)

A

10^9

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13
Q

Factor of a metre: Ångstrom (Å)

A

10^-10

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14
Q

Beer-Lambert Law

A

A=Ɛcl
where A=absorbance Ɛ=molar absorption coefficient at given l (M^-1cm^-1) c=concentration (M) l=distance light passes through sample (cm)

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15
Q

Bronsted-Lowry theory

A

For every acid there is a conjugate base

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16
Q

pH in terms of [H+]

A

pH=-log10[H+]
acidic solutions: [H+] > 1x10^-7M pH < 1x10^-7M pH >7
neutral solutions: [H+] = 1x10^-7M pH =7

17
Q

equilibrium constant expression for aA + bB = cC + dD

A

Ka = ([C]^c[D]^d)/([A]^a[B]^b)
If K >1 product favoured
If K <1 reactant favoured

18
Q

pKa in terms of Ka

A

pKa = -log10Ka

19
Q

Henderson-Hasselbach equation

A

pH = pKa + log10[base]/[acid]

20
Q

Le Chatelier’s principle

A

If a reaction mixture at equilibrium is disturbed, reaction occurs in the direction that opposes the change

21
Q

First order rate law for aA + bB = cC + dD

A

v=k[A]^x[B]^y

22
Q

First order concentration-time equation

A

ln[A]t=ln[A]o-kt

23
Q

Second order rate law for aA + bB = cC + dD

A

v=k[A]^2

24
Q

Second order concentration-time equation

A

1/[A]t = kt+ 1/[A]o

25
Q

First order half life equation

A

ln2 = kt1/2

26
Q

Second order half life equation

A

t1/2 = 1/(k[A]o)

27
Q

Arrhenius equation

A

lnk = lnA - Ea/RT

where A=prefactor Ea=activation energy R=gas constant (8.314Jmol^-1K^-1) T=temp in Kelvin

28
Q

Gibbs free energy

A
ΔG = ΔH - TΔS
if ΔG > 0 spontaneous
if ΔG < 0 non-spontaneous
if ΔG = 0 equilibrium
G = gibbs free energy (energy available to do work) H= enthalpy (the conversion of potential energy to heat) T = temp in Kelvin S = entropy (molecular disorder)
29
Q

free energy and chemical equilibria

A

ΔG = -RTlnK
if K > 1 spontaneous
if K < 1 non-sponataneous
if K = 1 equilibrium

30
Q

Boltzmann equation

A

S = Kb lnW

where S is entropy, Kb is Boltzmann’s constant (1.38x10^-23K^-1) W is the number of ways a state can be acheived

31
Q

First law of thermodynamics

A

Energy can neither be created nor destroyed but merely converted from one form to another

32
Q

Second law of thermodynamics

A

In any spontaneous process the entropy of a system and its surroundings always increases

33
Q

third law of thermodynamics

A

The entropy of a perfect crystal at absolute zero is zero

34
Q

Cell potential

A

ΔG = -nFE
where n is number of moles of electrons
F is Faraday constant (96485C/mol)
E = cell potential (V)

35
Q

Nernst equation

A

E = E°cell - (RT/nF)lnQ

Q is the reaction quotient