Practical questions Flashcards

(28 cards)

1
Q

How does increasing the mass of CaCO3 added affect the gas volume?

CP1- Measure the molar volume of gas

A

. If in excess, no effect
- if liimiting reagent> will increase

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2
Q

Possible errors? How to pattern?

CP1- Measure the molar volume of gas

A

Some gas can escape before bung is replaced to conical flask : seal apparatus using gas syringe or bung
- Bung not airtight
- Some CaCO3 lost whilst transferring from weigh boat to conical flask
- CO2 is slightly soluble in water > exact volume not measured

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3
Q

Why do you need to be quick when transferring the CaCO3 to the boiling tube + replacing the bung?
Why is a mass of above 0.04g not used?

CP1- Measure the molar volume of gas

A

To minimise gas loss
.Use of over 0.40 g of calcium carbonate will result in the volume of gas produced exceeding the capacity of the measuring cylinder.
-If larger masses of calcium carbonate are to be used then a larger measuring cylinder will be required.

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4
Q

How do you prevent gas escaping?

CP1- Measure the molar volume of gas

A

Place the solid reactant upright inside a sample tube in the conical flask, tipping the tube over by moving the conical flask around to start the reaction

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5
Q

CP2- use a standard solution to find the concentration of a solution of

Why is there no need to dry the conical flask after washing it out between trails?

sodium hydroxide.

A

the water will not change the number of moles of NaOH as this is measured before it is put into the flask

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6
Q

Why should the pipette be rinsed with sodium hydroxide solution after washing it with water?

A

water left in the pipette will dilute the sodium hydroxide, changing the number of moles used

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7
Q

What can be concluded by this practical?

CP1- Measure the molar volume of gas

A

smaller chips will have a large surface area and so will react more vigourously
with powdered chips having the fastest rate of reaction.

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8
Q

explain method

CP4- rates of hydrolysis of halogenoalkanes

A

rate of hydrolysis depends on the halogen atom on the haloalkane

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9
Q

steps

A
  1. add 1cm^3 of ethanol to each test tube
  2. next we add 0.1cm^3 of haloalkane to each test tube, 1-chloropentane, 1-bromopentane, 1-iodopentane
  3. Now place test tube in 60C degree water bath
    At cooler temperatures, hydrolysis is very slow.
  4. In a separate test tube, we add aqueous silver nitarte
  5. we then place this in a separate test tube in the same waterbath
  6. we now wait for 10 minutes for all of the solutions to reach the same temperature
  7. Now we add 1cm^3 of aqueous silver nitrate to each test tube and start timing.
    ‘aqueous’ water is acting as a nucleophile and reacts with the haloalkanes. hydrolysis takes place.

Halide ions are relased and react with silver ions
eg
Cl-(aq) + Ag+(aq) —> AgCl(s)
silver chloride- white precipitate
silver bromide- cream precipitate
silver iodide precipitate

chlorine will be the slowest as it has a high bond enthalpy. so takes a lot energy to break carbon to chloriine bond.

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10
Q

why do we use ethanol

A

haloalkane is insoluble in water.

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11
Q

(i) State the purpose of adding ethanol to each of the test tubes.

A

acts as a solvent
to dissolve both halogenoalkane

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12
Q

Give one reason why the test tubes were put in the same beaker of hot water.

A

so they reach same temperature

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13
Q

Give one reason why the test tubes were shaken after the addition of aqueous silver
nitrate.

A

to ensure reactants are mixed thoroughly

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14
Q

State how the halogen atom present in each halogenoalkane can be identified using
observations from this experiment in (a).

A

chloride-white ppt
bromide-cream ppt
iodide-yellow ppt

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15
Q

Identify further reagents that can be added, including relevant observations, to
confirm the identity of the halogen atom present in each halogenoalkane.

A

dilute and concentrated ammonia solution

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16
Q

Tests for aldehydes

A

2.5cm^3 AgNO3
1 drop NaOH
NH3 (aq) dropwise with agitation until precipitate dissolves
Hot water
mix the test tube with 2cm^3 of sample
wait 15 mins for silver mirror to form

17
Q

Tests for carboxylic acids

A

2cm^3 sample
3-4 drops of NaHCO3(aq)
observe bubbling/fizzing

18
Q

Tests for haloalkanes

A

100 cm3 boiled water
10 drops sample
2 cm3ethanol
2.5 cm3AgNO3(aq)
Warm –5 minutes
Mix solutions
Observe any precipitates

19
Q

Tests for hydrocarbons

A

3–4 drops sample
1 cm3Br2(aq)
Agitate the tube
Observe bromine
water turning
colourless

20
Q

Tests for alcohols

A

3–4 drops Cr2O72-/ H+
3–4 drops sample
orange to green

21
Q

Aspirin synthesis

A

https://www.youtube.com/watch?v=0iKtr3xXEj8&t=745s

22
Q

reaction pathways

23
Q

Oxidation of ethanol

A

Add acidified potassium dichromate solution in a pear shaped flask
Cool down the flask
Add a few anti bumping granules (prevent formulation of large bubbles) add ethanol drop wise to pear shaped flask
Warm flask To room temperature

24
Q

Why do add ethanol drop by drop in CP5

A

Allows controlled reaction observation of intermediates

25
Practical 8 Determination of enthalpy change using Hess’s Law. Polysteyrene cup
Method 1. Place one of the reactants into a polystyrene cup and place a thermometer with it. 1. Start a stopwatch and record the temperature of the liquid every minute. 2. At 4 minutes, add the second reactant and dont record a temperature change for this minute. 3. At 5 minutes continue taking temperature readings each minute for a further ten 4. Plot temperatures of a graph and extrapolate to find AT. 5. Repeat for the second reaction. Key Points • Q = mcAT, where m = mass of the solution, c = specific heat capacity, AT = change in temperature. • AH = Q/moles,
26
# CP-16 Synthesis of aspirin Describe, in outline, how a sample of a solid, is purified by recrystallisation 4 marks
1 dissolve (impure product) in a minimum volume of hot solvent (1)  M2 cool (in ice) or leave to recrystallise (1)  M3 filter using vacuum filtration / Buchner filtration / filter under suction (1)  M4 dry solid in desiccator / between filter papers (1)
27
process of synthesis of aspirin
weigh 6 grams of salicylic acid using a balance tip into conical flask reweigh using a weighing point eg 5.97g add 10cm^3 ethanoic anhydride add 5 drops of phosphoric acid warm for 20 minutes add ice cold water (water bath) - washes away impurities, causes solids to clump together. increasing yield filter of crude aspirin using a vacuum pump leave to dry weight and calculate yield recrytallisation impure organic solid (you have insoluble impurities + soluble impurities) dissolve (impure product) in a minimum volume of hot solvent (1)  M2 cool (in ice) or leave to recrystallise (1)  M3 filter using vacuum filtration / Buchner filtration / filter under suction (1)  M4 dry solid in desiccator / between filter papers using melting point aparastus measure the melting point of aspirin should be close if you have pure aspirin. 136 dgrees c
28
Why is concentrated sulfuric acid used when synthesising aspirin?
Used as a catalyst to increase the rate of reaction