Chaotwr 18 Flashcards

1
Q

What is rate of reaction formula

Units

A

CHANGE IN Concentration / time

CAN be increase conc if a product or decrease conc if a reactant

In which case the graph Will start high finish low

2) units = moles-3 s-1

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2
Q

Orders

A

This is if doubke conc and order is one, the rate double 2 too, if doubke and order 2, then sqaure

If doubling has no effect, rate is 0

Overal, rate is the sum of the indicies in rate equation

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3
Q

How to compare orders question

How to find k?

A

Say comparing reaction 1 and 2, and say how one thing is constant (or work it out to be constsnt)

When conc increase y, rate increase by, therefore the order of reactions I x with respect to y

2; find k by once write rate equation sub a row in

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4
Q

Why do we need continous methods of monitoring to find conc time graphs WHATS the use?

A

As conc/ time = rate, the gradient tells us the rate, and the change of gradient with respect to the conc will tell us the orders

Also with a conc time graph we can take instaneoues rates and use that to find RATES, that allow us to plot against conc for rate conc graph which gives us perfect picture

Can also maybe tell directly from a conc time graph the order, assuming everything else constsnt

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5
Q

SHAPES FOR CONC TIME

A

If it’s flat low= 0 order
- bevause the gradient is constsnt = rate is constant, doesn’t change with a change of conc

If it’s curved = 1
- gradient constantly changing, meaning with a change of conc the rate changes proprtinaly

If it’s even more curved = 2
- this because now change of conc will cause gradient to change by that factor sqaured
But we don’t need to know this

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6
Q

Why does 1st order conc time follow exponential decay?

How can we tell if it’s expoential usign half lives

A

Because for the same given time interval, the factor of decrease is CONSTANT

2) if the time taken for conc to drop to half is the SAME in successive jumps = expoential decay and FIRST ORDER

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7
Q

Why can there be two ways of rate EQUATUIN fir same reaction?

A

Once for the products and one for the reactants

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8
Q

How ti find the k constsnt assuming that rate equation only has ONE reactant and it has constant half life

A

K = ln2 / half life

OR 1) rate = k x
Find rate of x at any conc using gradient
And re arranbe

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9
Q

Shapes of rate conc and how to find k assuming only reactant

HOW TO PLOT RATE CONC GRAPH?

A

0 order straight , as conc increases nothing happens to rate

K = y intercept

1st = linear
As conc increase so does rwte, gradient = k

2nd = quadratic
And if you plot rwte/ conc 2, gradient will be the k

2) to plot a rate conc graph, need to find gradients of conc time graph at different concentrations and record them!

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10
Q

How ti do continous monitoring experiments which type

Why do we use mass decrease when clearly a gas is produced?

A

1). Monitoring as mass decreases with time (
2) monitoring the increase in volume / time (upturned flask ) for something that produces gas/ gas tube
NEED MASS DECREASES TECHNIQUE when the gas being produced DISSOLVES IN THE LIQUID, meaning you can’t collect it!

3) using colorimeter

Need Coleoptera because not all reactions produce a gas!

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11
Q

How to do these with Colorimtery

A

1st need to plot a calibration curve.

Of known concs of the product, test with colorimeter
- opposite wavkentgh of light
-zero with distilled water between esch redwing
- take readings of either absorbsnce transmittance whatever , cinc agsisnt this

Now at integrals take out samples of your thing, and measure the absorbsnce

Can now find concs at the different times, now have conc time graph

Can then go on to make a rate conc graph etc

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12
Q

What is the intial rates method and why is it better

WHAT IS ASSUMPTION

A

To find orders etc, you have to compare the INITAL RATES with different concentrations

This is tedious cuz it means you have to keep drawing new graphs

Instead if you observe the time taken for a colour change to happen, and assume that less than 15% of the reaction has happened, then you can make ASSUMPTION THAT THE INITAL RATE = TO THE RATE YOU CALCULATED

As the rate will be PROPORTIONAL to 1/t taken for a colour change to appear ( more conc = quicker rate = less time), you can use these values and plot against concentration to give you the SHAPE of the graph that will allow you to find the order of reaction very easily

However if you acc want to find k will need to do calculations to find concs

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13
Q

Again what is assumption with intial rates method

A

That the colour change took place e before 15% if reavtion done, because then the intial rwte is roughly the same as this rate

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14
Q

What happens in iodine clock?

A

First reavtion iodine is made
Second reaction reacts with thisulfste to go back to iodine ions

You have starch , and starch shoud remain colourless as iodine is converted till ions

Only until ALL THE THISUKFSTE IS USED, will the colour change happen and it remains BLUE as iodine is no longer converted

Reason for using thisukfste is because colour change would else happen STRAIGHT AWAY, it’s needed to delay

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15
Q

What side is the rate equation normally , reactant or product?

A

Normally reactant because you measure decrease in conc

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16
Q

Finally what to do once iodine clock set up actually to find how rwte changes

A

For each thing testing keep other concs constsnt.

CHNAGE conc of thing testing record time and find 1/t for each

The. L,lt and find rodees and make rwte equation

17
Q

Why does an increase in TEMPERTAURE increase the rate constant and RATE OF REAVTION gcse

A

1) increase temp, means particles increase ke and move around more, collide more, so number of succeful collisions increase, so they increase rate
2) also more particles have the required ACTIVISTION ENERGY needed for reaction to work so rwte increases

So for these reasons, EA and Collins js

But as we see collisions have less effect on rwte constsnt

18
Q

Why does activation energy play much more big role than Collins based on Arrhenius

A

Because collision just a constant whereas activation energy is exponaitlsed

19
Q

Increasing activisitonnemergy temp does what to k

A

As exponent, in reading ea will decrease as its negative

Snd increasing temp will increase as its -1/t so will increase the k

20
Q

What is the ONLY THING that contributed to K constsnt changing

A

TEMPERATURE

21
Q

Why do most reactions take place in a MULTI STEP RESCTION LATHWAY ARATHER THAN ONE

A

For reaction to occur
# must collide
- with required ea
- and CORREVT ORIENTATION

The probiotic of this happening when the number of particles exceed 2 are dramatically low

Thus it’s likely they occurs in multi step reavtion lathway instead e with 1 to 1 moles

22
Q

What is the rate detemrinignstep

A

The SLOWEST STEP IN REACTION PATHWAY

As it’s slowest, it determines the rate as it’s like limiting factor

Rwte Det Mei it step involves everything in rwte equation as those ultimately attribute to the rwte

23
Q

Rules

A

The moles of things in rwte determine step = number molecules

All the things in the rate equation must appear in rate determining step

Any intemrkdwte made must be destroyed

Can be multiply fast steps

Once removed all intermediates should cancel down to original ewaurion
LDONT BE AFRAID OF WACKY INTERMODATE

24
Q

Why can sometimes order of something effective be 0

A

If it’s in excess it will be 0 clearly doesn’t have an effect

If it stays the same after reavtion down probably just a cakcysyd

25
Q

Why does reaction not happen in one step

A

As unlikely collide same time originations rn ea

Not all feature in rwte equation

26
Q

Why can we NOT determined the order

A

Agsin in excess so varying conc is hard!!!

Or reaction doesn’t produce anything that allows continous skin toting