3.2.1 Enthalpy changes Flashcards

including measuring enthalpy changes spec. ref. = 3.2.1, 2.1.3 and Hess's Law and enthalpy cycle questions spec. ref. = 3.2.1

1
Q

what happens in an exothermic reaction

A

energy is released causing the temperature of the surroundings to increase

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2
Q

describe the enthalpy change profile of an exothermic reaction

A

Energy is released
SO products are lower in energy than reactants
SO enthalpy change (𝚫H) is negative

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3
Q

What happens in an endothermic reaction

A

Energy is absorbed causing the temperature of the surroundings to decrease

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4
Q

Describe the enthalpy change profile of an endothermic reaction

A

Energy is absorbed
SO products are higher in energy than reactants
SO enthalpy change (𝚫H) is positive

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5
Q

desribe the enthalpy change (𝚫H) arrow on an enthalpy profile

A

The arrow goes from the reactants to the products it will be up for endothermic (+ve) reactions and pointing down for exothermic reactions (-ve)

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6
Q

what is activation energy (Ea)

A

Activation energy is the minimum amount of energy required to start a reaction (by breaking bonds)

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7
Q

Describe the activation energy (Ea) arrow on an enthalpy profile

A

The arrow always goes up. it goes from the same level as the reactants to the top of the arch (therefore needing to be in the middle NOT on the reactant line)

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8
Q

What 2 equations are used to calculate 𝚫H

and in what order

A

Q = mc𝚫T
then 𝚫H = Q/n

energy = mass of water x specific heat capacity x the change in temperature
enthalpy change = energy divided by number of moles

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9
Q

what are the units for Q = mc𝚫T

A

Joules = grams x (J/g/℃) x ℃

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10
Q

what

what are the units for 𝚫H = Q/n

A

(KJ/mol) = joules x number of moles

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11
Q

what is the equation for 𝚫H using the enthalpy of the products and reactants

A

𝚫H = H(products) - H(reactants)

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12
Q

what is the law of the conservation of energy

A

energy cannot be created or destroyed

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13
Q

what is this symbol for 𝚫H⦵

the ⦵ should be smaller and in the top right (superscript)

A

standard enthalpy change

takes place under standard conditions

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14
Q

what are standard conditions

A
  • components in their standard states
  • standard conditions:
    298K
    1atm (101kpa)
    1moldm⁻³
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15
Q

what is 𝚫H⦵r for

the r would normally be in the bottom right (subscript)

A

standard enthaply change of reaction

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16
Q

define standard enthalpy change of reaction

A

enthalpy change that accompanies a reaction in the molar quantities shown

17
Q

what is 𝚫H⦵c for

the c would normally be in the bottom right (subscript)

A

standard enthaply change of combustion

18
Q

define standard enthalpy change of combustion

A

enthalpy change when 1 mol of a substance completely reacts with O₂

19
Q

what is 𝚫H⦵f for

the f would normally be in the bottom right (subscript)

A

standard enthalpy change of formation

20
Q

define standard enthalpy change of formation

A

enthalpy change when 1 mol of a substance is formed from its elements in their standard states

21
Q

what is 𝚫H⦵neut

the neut would normally be in subscript

A

standard enthalpy change of neutralisation

22
Q

define standard enthalpy change of neutralisation

A

enthalpy change when an acid and a base react to form 1 mol of water

23
Q

state Hess’s Law

A

The enthalpy change of any 2 route is the same as long as the initial and final states are the same

24
Q

what does Hess’s Law do

A

Hess’s law provides a way of measuring 𝚫H indirectly

25
Q

why can some 𝚫H not be measured directly

A
  • they have a very high Ea
  • the reaction is very slow
  • there are a mixture of side reactions or products
26
Q

How do you calculate 𝚫H using 𝚫Hf data

𝚫H of say reaction - not that important to the question

A

𝚫Hr = - 𝚫Hf(reactants) + 𝚫Hf(products)
OR
𝚫Hr = 𝚫Hf(products) - 𝚫Hf(reactants)

they are the same just different ways around

27
Q

How do you calculate 𝚫H using 𝚫Hc data

A

𝚫Hr = 𝚫Hc(reactants) - 𝚫Hc(products)

28
Q

how do you convert from kelvin to ℃

A

add 273 to the ℃

29
Q

using a spirit burner

describe an experiment that gives 𝚫Hc data

A

liquid fuels such as methanol can be burned easily using a small spirit burner.
1. Using a measuring cylinder, measure out 150cm³ of water. pour the water into the beaker and record the initial temperature of the water ( to the nearest 0.5℃)
2. Add methanol to the spirit burner. weigh this and record the mass.
3. place the spirit burner under the beaker, and light it whilst stiring the water with a thermometer.
4. after ~3mins extinguish the flame. Immediately record the maximum temperature reached by the water
5. reweigh the spirit burner with methanol in and assume the wick has not been burned

As the water has gained energy the methanol must have lost the same amount of energy so the 𝚫H is negative and the reaction exothermic - keep in mind for Q calculation and then the 𝚫H calculation use this symbol at the end to check

30
Q

why may experimental 𝚫Hc data be inaccurate

A
  • there is heat loss to the surroundings other than water (this includes the beaker but maining the air surrounding the flame)
  • incomplete combustion of methanol
  • evapouration of methanol from the wick ( the burner must be weighed immediately after extinguishing the flame, otherwise some methanol my evapourate - spirit burners usually have a cover to minimise this)
  • Non-standard conditions