Thermochemistry Flashcards

1
Q

Thermochemistry

A

heat changes of chemical reactions
helps to determine if a particular reaction will occur and if it will release or absorb energy as it occurs

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2
Q

two principles of thermodynamics

A

Laplace law
Hess’ Law

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3
Q

The Laplace Law

A

the heat change (or enthalpy change) of a chemical reaction is exactly equal but opposite in sign for the reverse reaction
∆Hforward reaction = ∆Hbackword reaction
(a) CH4 (g) + 2O2 (g) → CO2 (g) + 2H2O (l) [here, ∆H0 = -890.3 kJ mol-1]
(b) CO2 (g) + 2H2O (l) → CH4 (g) + 2O2 (g) [here, ∆H0 = +890.3 kJ mol-1]

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4
Q

Enthalpy Notations

A

enthalpy change 𝚫H(delta H) is the heat energy transferred in a reaction at constant pressure. The units are Kj mol⁻1

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5
Q

Standard conditions (𝚫Hᶿ)

A

100 kPa pressure and a stated temperature

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6
Q

Energy

A

stored in the bonds of chemical compounds.
Chemical energy may be released during a chemical reaction, often in the form of heat; such reactions are called exothermic.

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7
Q

Work

A

transfer of mechanical energy between two systems

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8
Q

Heat

A

transfer of thermal energy between systems

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9
Q

Exothermic reactions

A

have a negative enthalpy change value, because heat is given out (the chemicals lose energy)

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10
Q

Endothermic reactions

A

have a positive enthalpy change value, because heat energy is absorbed (the chemicals lose energy)

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11
Q

Lattice formation enthalpy

A

enthalpy change when 1 mole of a solid ionic compound is formed from its gaseous ions

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12
Q

Lattice dissociation enthalpy

A

enthalpy change when 1 mole of a compound is formed from its elements in their standard states

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13
Q

Bond dissociation enthalpy

A

enthalpy change when all the bonds of the same type in 1 mole of gaseous atoms are broken

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14
Q

First ionisation energy

A

enthalpy change when 1 mole of gaseous 1+ ions is formed from 1 mole of gaseous atoms

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15
Q

First electron affinity

A

enthalpy change when 1 mole of gaseous 1- ions are made from 1 mole of gaseous ions

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16
Q

three types of thermodynamics systems

A

open
closed
isolated

17
Q

isolated system

A

thermodynamic system that cannot exchange either energy or matter outside the boundaries of the system
1. The system may be so distant from another system that it cannot interact with them.
2. The system may be enclosed such that neither energy nor mass may enter or exit.

18
Q

Closed systems

A

only closed to matter, energy can be exchanged across the system’s boundaries

19
Q

Open system

A

exchange both energy and matter with its surroundings

20
Q

Hess’ Law

A

The enthalpy change accompanying a chemical reaction is independent of the route by which the chemical reaction occurs.

21
Q

1st law of thermodynamics

A

a systems energy content remains constant as well as not being able to be created or destroyed

22
Q

Activation energy

A

minimum energy required

23
Q

Increase temp effect on Maxwell-Boltzmann diagram

A

move right

24
Q

Reaction Rate for a given chemical reaction

A

measure of the change in concentration of the reactants or the change in concentration of the products per unit time

25
Q

speed of a chemical reaction

A

change in concentration of a substance divided by the time interval during which this change is observed

26
Q

Rate formula

A

change in concentration (of products or reactants)/ time

27
Q

Reaction rate and concentration

A

increases
more of the reacting molecules or ions are present to form the reaction products
limit is often reached where increasing the concentration has little effect on the rate of reaction.
When several reactants are involved, increasing the concentration of one of them may not affect the rate of reaction if not enough of the other reactants is available

28
Q

Reaction rate and Temperature

A

increases
Particles can only react when they collide
heat a substance, the particles move faster and so collide more frequently
disproportionately large increase in the number of high energy collisions. It is only these collisions (possessing at least the activation energy for the reaction) which result in a reaction.

29
Q

Reaction rate and Surface Area + on graph

A

cutting the substance into small pieces, or by grinding it into a powder
more particles are exposed to the other reactant
there are more collisions
the rate of reaction increases

has a steeper gradient at the start
becomes horizontal sooner

30
Q

half-life of a reaction

A

amount of time needed for a reactant concentration to decrease by half compared to its initial concentration
used in chemistry and medicine to predict the concentration of a substance over time

31
Q

concepts of half life plays a key role in

A

administration of drugs into the target, especially in the elimination phase, where half life is used to determine how quickly a drug decrease in the target after it has been absorbed in the unit of time (sec, minute, day,etc.) or elimination rate constant ke (minute-1, hour-1, day-1,etc.).

32
Q

Zero order kinetics

A

rate of a reaction does not depend on the substrate concentration
slope of this plot is a straight line with negative slope
the half-life of zero order reaction decreases as the concentration decreases

33
Q

First Order Kinetics

A

slope continually decreases as time progresses until it reaches zero
the length of half-life will be constant, independent of concentration
takes the same amount of time for the concentration to decrease from one point to another point

34
Q

Second Order Reactions

A

decrease at a much faster rate
length of half-life increases while the concentration of substrate constantly decreases, unlike zero and first order reaction

35
Q

rate equation

A

rate = k [A]a [B]b

shows the effect of changing the concentrations of the reactants on the rate of the reaction

36
Q

rate constant

A

only changes if conc changes

37
Q

The Arrhenius equation

A

k = Ae ^Ea/RT

38
Q

gas constant

A

constant which comes from an equation, pV=nRT, which relates the pressure, volume and temperature of a particular number of moles of gas

39
Q

Activation energy, EA units

A

joules per mole