lecture 4 Flashcards

1
Q

what is a standard state

A

the most usual form at 1 bar pressure and a specified temperature (298.15K)

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2
Q

how is enthalpy in non standard conditions calculated

A

H = H* + correction

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3
Q

what is H*

A

enthalpy at standard conditions

1 bar pressure
298.15K temp

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4
Q

what is standard enthalpy change

A

triangle H*

enthalpy change for a process where the initial and final substances are in their standard states

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5
Q

standard state for o2

A

gas

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6
Q

standard state for h2o

A

liquid

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7
Q

standard state for C

A

solid graphite

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8
Q

what is the enthalpy of formation

A

triangle f H*

enthapy change associated with forming a molecule from its constituent elements in their standard states

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9
Q

what is the enthalpy of formation of ‘x’ in their standard states

A

0

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10
Q

what is the enthalpy of formation when smt is formed but their constituent elements were not in their standard states

A

not 0

it has a value

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11
Q

what is enthalpy of vaporization

A

triangle vH*

enthalpy change when smt goes from liquid to gas under standard conditions

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12
Q

what is enthalpy of combustion

A

triangle cH*

oxidation of ‘x’ with o2 gas to give co2(g) and h20 (l)

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13
Q

what is enthalpy of solution

A

triangle sH*
separation of + and - ions in water

infinite dilution limit

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14
Q

hess law definition

A

standard enthalpy of a given reaction can be obtained as the sum of standard enthalpies for a sequence of reactions when we start with the same rea and end with the same pro.

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15
Q

what is standard enthalpy change of a reaction

A

pro - rea

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16
Q

hess law broken down

A

rea

standard state elements

pro

17
Q

what is a born haber cycle

A

closed path of transformations starting and ending at the same point

18
Q

what temp were enthalpy changes recorded at

A

a couple but definitely not all

19
Q

how can we determine the enthalpy of a substance at any given temp

A

use the substances specific heat capacity

20
Q

equation to find enthalpy of substance at temp 1 when we know enthalpy at temp 0

A

H (T1) =
H (T0) + integral of Cp dT

integral limits =
T1 top
T0 bottom

21
Q

what is kirchhoffs law

A

enthalpy change of reaction at temp 1 = enthalpy change of reaction at temp 0 + intgral of the specific heat capacity multiplied by dT)

integral: t1 top t0 bottom

22
Q

the change in specific heat capacity of a reaction is

A

total specific heat capacity of products - total specific heat capacity of reactants

including the stoichiometry (molar ratio)

23
Q

what does kirchhoffs law help us do

A

helps us calculate the enthalpy change for a reaction at any temp when we know the enthalpy change at one temp + the heat capacities of the rea and products

24
Q

change in Cp

A

specific heat of pro - specific heat of rea

25
Q

temp change

A

final temp - intial temp

26
Q

actual heat capacity variations equation

A

H(T1) = H(T0) + integral Cp dT

integral upper limit = t1
integral lower limit = t0

area under graph = enthalpy change of the substance

plot of cp against temp

diff phases = diff heat capacities

27
Q

how can we measure enthalpy change

A

use differential scanning calorimetry

DSC

28
Q

how does DSC work

A

differential scanning calorimetry

  • increase temp in a sample with a reference that doesnt change
  • measure changes in heat capacity at a constant pressure
  • enthalpy change is equal to the area under the curve when Cp is plotted against temp
29
Q
A