formulas Flashcards

(35 cards)

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

24
Q

Second order concentration-time equation

A

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

25
First order half life equation
ln2 = kt1/2
26
Second order half life equation
t1/2 = 1/(k[A]o)
27
Arrhenius equation
lnk = lnA - Ea/RT | where A=prefactor Ea=activation energy R=gas constant (8.314Jmol^-1K^-1) T=temp in Kelvin
28
Gibbs free energy
``` 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
free energy and chemical equilibria
ΔG = -RTlnK if K > 1 spontaneous if K < 1 non-sponataneous if K = 1 equilibrium
30
Boltzmann equation
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
First law of thermodynamics
Energy can neither be created nor destroyed but merely converted from one form to another
32
Second law of thermodynamics
In any spontaneous process the entropy of a system and its surroundings always increases
33
third law of thermodynamics
The entropy of a perfect crystal at absolute zero is zero
34
Cell potential
ΔG = -nFE where n is number of moles of electrons F is Faraday constant (96485C/mol) E = cell potential (V)
35
Nernst equation
E = E°cell - (RT/nF)lnQ | Q is the reaction quotient