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Constants and Key Equations in Chemicall Reaction

This document lists important constants, equations, and relationships that are useful for understanding chemical reactions. Some key equations included are: - Ideal gas law: PV=nRT - Gibbs free energy: G=H-TS - Equilibrium constant expressions: Ka, K', Ksp - Standard transformed equations: ΔG°=-RTlnK, ΔG=ΔG°+RTlnQ - Reaction rate expressions: Rate = k[A]a[B]b, Arrhenius equation

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Francisca Braz
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0% found this document useful (0 votes)
40 views

Constants and Key Equations in Chemicall Reaction

This document lists important constants, equations, and relationships that are useful for understanding chemical reactions. Some key equations included are: - Ideal gas law: PV=nRT - Gibbs free energy: G=H-TS - Equilibrium constant expressions: Ka, K', Ksp - Standard transformed equations: ΔG°=-RTlnK, ΔG=ΔG°+RTlnQ - Reaction rate expressions: Rate = k[A]a[B]b, Arrhenius equation

Uploaded by

Francisca Braz
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Constants and key equations in Chemical Reaction

Name Symbol Value (in SI units)

Avogadro’s number NA 6.0221367 · 1023 mol-1

Boltzmann’s
constant k 1.380658 · 10-23 J · K-1

Faraday’s number F 9.64853 · 104 C · mol-1

Ice melting point (1 atm) Tis 273.15 K

Speed of light in vacuum c 2.99792 · 108 m · s-1

Planck’s konstant h 6.626075 · 10-34 J · s

Gas constant R 8.3145 J · K-1 · mol-1


= 1.987 cal · K-1 · mol-1
= 0.08206 L · atm · K-1 · mol-1

Interconversion between units:

1 cal = 4.184 J
1 Volt · coulomb = 1 J
1 L · atm = 101.325 J = 24.217 cal
1 Å = 10-10 m
1 mm Hg (or 1 Torr) = 133.322 J · m-3
1 atm = 760 mm Hg = 101325 Pa
1 J = 107 erg
Mathematical Equations

Straight line y = ax + b
Logarithmic rules ln(a·b) = ln a + ln b ln(a / b) = ln a – ln b

ln(ar) = r ln a ln a = ln 10 · log10 a

Differential relations
Function f(x) Derivative of function f´(x)
ln x x-1
ex ex
ekx k · ekx
ax ax · ln a
xa a · xa-1
x-1 -x-2
!
√𝑥 = x½ "√$
= ½x-½

Integration of functions

Function f(x) Stem function ∫ f(x)dx

ln x x ln x - x
ex ex
1 kx
ekx k
e

ax
ax
ln a
1
xa a+1
xa+1

x-1 ln |x|
2 3
√x = x½ x2
3
Physical chemistry equations – “our tool box”

n = m/M N = Na·n

%
c = n/V 𝑋i = ∑ %i
i i

Ideal gas law


P - pressure n - number of moles PV=nRT Pi = xi · Ptotal
R - gas constant T - temperature
V-volume

ΔU = q + w H =U+PV

G = H – TS d G = –S d T + V dP

dw = -Pex dV ΔH = ΔU + Δng RT

G(ci) = Gi° + RT lnci G(Pi) = Gi° + RT lnPi

dqrev
dS = T
ΔH = qP ΔU = qV

ΔF = F(final state) – F(initial state)

∂U ∂H
CV = ( ∂T ) CP = ( ∂T )
V P

γ γ
cC ∙ cδD δ
cC ∙ cD
∆G = ∆G° + RT lnQ Q = + α ∙ c β, Ka = + α ∙ cβ ,
cA B cA B
not equilibrium equilibrium

∆G
∂∆G ∂4 5 ∆H
∆G = ∆H + T ( ∂T ) - T
. =-
P ∂T T2
P
a H+ ∙ a A- corg
Ka = aHA
aH+ ∙ aOH- = Kw K' = cw

∆𝐺 = ∆𝐻 - 𝑇∆𝑆 -∆r 𝐺° = 𝑅 𝑇 ln 𝐾a

d ln 6a ∆ 8°
r 6 ∆r 8° 1 1
d7
= 97 "
ln 62 = - 9
(7 - 7 )
1 2 1

7
∆r 𝐻°(𝑇2 ) = ∆r 𝐻°(𝑇1 ) + ∫7 2 ∆r 𝐶P d𝑇
1

: ∆8(evaporation) 1 1
ln 2 = - ( - ) or ∆𝐻(sublimation)
:1 9 72 71

∆8(transition)
∆𝑆 = 7(transition)
∆𝐺(𝑒𝑞) = 0

𝑃A = 𝑋A ∙ 𝑃A* Δ𝑃 = 𝑋; ∙ 𝑃<∗

97 " 97 2
∆𝑇b = ∆8(fordampning)
#
∙ 𝑋2 ∆𝑇f = ∆8(smelte)
f
∙ 𝑋2

∆𝑇b = 0.51 ∙ 𝑚 ∆Tf = 1.86 ∙ 𝑚

𝜋 = 𝑐 𝑅 𝑇

𝑃; = 𝐾 ∙ 𝑋; 𝑃; = 𝐾´ − ∆> 𝐺° = 𝑅 𝑇 ln 𝐾? 𝑚;

v = k(T)[A]a [B]b k(T) = A ∙ exp(-Ea/RT)

𝑘" 𝐸𝑎 1 1
ln = − + − ,
𝑘! 𝑅 𝑇" 𝑇!
EMF= Eright – Eleft EMF°= E°right – E°left Electromotive force and standard electromotive force
constants for the cell potential at 25ºC on page 526 in
pdf version
∆r 𝐺° = -𝑅 𝑇 ln 𝐾a = −𝑛 𝐹 𝐸𝑀𝐹°

97 ["ox"] FGHI ["ox"]


𝐸 = 𝐸° + %@ 𝑙𝑛 ["red"] 𝐸 = 𝐸° + %
𝑙𝑜𝑔 ["red"]

Q= It=nzF

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