3.2 Flashcards

1
Q

define enthalpy

A

the thermal energy stored in a chemical system. we can measure this by seeing if the temp of a reaction changes

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2
Q

how you know a Reaction has taken place

A

color change, effervescence, precipitate formed, temp/energy change

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3
Q

exothermic reactions

A

give out energy to their surroundings, make things feel hot, the energy of the products is less than that of the reactants

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4
Q

endothermic reactions

A

take in energy form their surroundings, make things feel cold, the energy of the products is greater than that of the reactants

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5
Q

activation energy

A

the energy needed to start breaking the bonds in the reactants. the minimum energy needed for a reaction to take place

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6
Q

how to calculate enthalpy change

A

enthalpy to break bonds - enthalpy to make bonds

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7
Q

negative enthalpy change means the reaction is

A

exothermic

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8
Q

positive enthalpy change mean the reaction is

A

endothermic

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9
Q

enthalpy change of neutralisation

A

(delta H neut) enthalpy change when one mole of water is formed from a neutralisation reaction can be exothermic or endothermic

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10
Q

enthalpy change of formation

A

(delta H f) enthalpy change when one mole of a compound is formed from its elements in their standard state usually exothermic

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11
Q

enthalpy change of combustion

A

(delta H c) enthalpy when one mole of a substance reacts completely with O2 always exothermic

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12
Q

standard conditions for enthalpy changes of reactions

A

pressure- 100 kPa (1 atm)

room temp- 289k (25`c)

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13
Q

measuring enthalpy change experimentally

A
Q=mcT 
T=temp change
c=specific heat capacity of substance being heated
m= mass of object being heated
Q=heat lost or gained from reaction in J
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14
Q

Hess’s law

A

The total enthalpy change of a reaction is independent of the route by which the reaction takes place provided the initial and final condition are the same

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15
Q

to increase the rate of reaction

A

increase pressure, increase surface area, increase temp, add a catalyst, increase concentration, increase surface area

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16
Q

why increase surface area

A

after rate of reaction as more particles are exposed and able to react

17
Q

why use a catalyst to increase rate of reaction

A

lowers the activation energy

18
Q

why increase the concentration

A

more particles per unit volume increase the chances go a successful collision

19
Q

rate of reaction

A

change in concentration of x over time

20
Q

two types of catalysts

A

heterogeneous catalyst, homogenous catalyst

21
Q

heterogenous catalyst

A

catalyst is in a different phase to the reactants i.e. solid catalyst vs gaseous reactants

22
Q

homogeneous catalyst

A

catalyst is in the same phase as the reactants i.e. all liquid or gaseous

23
Q

benefits of catalysts in general

A

increase sustainability, reduce temp needed -> cheaper

24
Q

Botzmann distribution

A

shows the distribution of molecules of certain energies, area under the curve= no. pf molecules in the system, if the temp is increased the curve becomes broader and flatter

25
Q

Le Chateliers principle

A

if conditions change the position of the equilibrium will respond by also changing to minimise the change imposed

26
Q

factors affecting the position of the equilibrium

A

concentrations reactants of products, pressure, temperature

27
Q

how concentration affects the equilibrium position

A

if the either the products or reactants concentrations are changed the rate of the forwards/backwards reaction will increase to minimise the change

28
Q

how pressure affects the equilibrium position

A

increasing the pressure favours the side with the lease moles

29
Q

how temperature affects the equilibrium position

A

one of the reactions (forward or backwards) will be exothermic and the other endothermic increasing temp favours the endothermic reaction, decreasing it the exothermic reaction

30
Q

equilibrium constant kc

A

kc>1 equilibrium to the right kc<1 to the left

31
Q

how to calculate the equilibrium constant

A

concentrations of products to the power of no. of moles divided by concentrations of reactants to the power of no. of moles