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Tukkay lagao musalmanoo Q9
http://papers.xtremepapers.com/CIE/...d AS Level/Chemistry (9701)/9701_w07_qp_1.pdf
http://papers.xtremepapers.com/CIE/...d AS Level/Chemistry (9701)/9701_w07_qp_1.pdf
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Thanku minion!
Metanoia
Yes, it must decompose, but can u include the temperature or for how long it must be heated, because even after heating for an hour, we couldnt find any loss in mass!
Please can u ask ur teacher about the temp and time it will be taking for decomposing? We couldnt get to anything
An autocatylsed reaction is when one of the products is actually a catalyst.
The rate of reaction :
starts off slow (no catalyst)
then increases (catalyst)
then decreases (concentration of reactants decreases)
In general, to estimate the "Mr of a gas mixture containing A and B", we use (% of A x Mr of A) + (% of B x Mr of B)
Using D as example,
D. (0.825 x 2) + (0.152 x 4) + (0.023 x 16) = 2.626
Doing a quick calculation and comparing to the other options will give D as the highest "Mr", meaning most dense gas mixture.
The two structures on the right are more obvious since they are acids which reacts with NaOH to form a carboxylate salt.
The two structures on the left are left out by students. They are esters which can undergo alkali hydrolysis to form a carboxylate salt and alcohol.
Carbon is more obvious as it has four valance electrons to form 4 covalent bonds.
Nitrogen can also form 4 bonds (3 single bonds and 1 dative bond), for example in NH4+
http://papers.xtremepapers.com/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_s03_qp_1.pdf
Please can you explain questions 1, 2, 7, 10, 21, 22, 23, 37 and 39?
The answers are A,B,D,B,D,D,B,B,C.
Q11. A) Ammonium ethanoate is not completely ionised in water and it's not acidic in aqueous solution. Water is more polar than ammonia, so the only choice left is that ammonia is a stronger base than water
Q30. D) When propanone reacts with hydrogen cyanide, nucleophilic addition takes place and a hydroxynitrile is formed.
CH3COCH3 + HCN → CH3C(OH)CH3CN
2-hydroxybutanenitrile is hydrolysed under acidic conditions to Butanoleic acid
CH3C(OH)CH3CN + H2O + H+ → (CH3)2C(OH)CO2H + NH4
Q31. C) Silicon tetrachloride doesn't have co-ordinate bonding because it follows the octet rule, sharing all of its valence electrons with the chlorine atoms.
Both silicon and chlorine are non-metals, so, it has covalent bonding.
There are instantaneous dipole-induced dipole forces between the molecules (Van der Waals forces)
Q32. A) The right-hand side of the structure is polar and since water is a dipole, it is attracted to water.
The alkyl chain is non-polar and attracted to other alkyl chains by Van der Waals forces. Since oil is of a similar character to this alkyl chain, the alkyl chain is soluble in oil droplets.
In alkanes, each carbon atom forms a tetrahedral structure (due to sp3 hybridisation), so the C-C-C bond angles are tetrahedral
Q33. A) The reaction is endothermic, which means that diamond has more energy than graphite. The enthalpy change of atomisation is the enthalpy change when one mole of gaseous atoms is formed from one mole of the element in the standard state. Since diamond has more energy than graphite, it requires a smaller enthalpy change of atomisation.
Since the enthalpy change of atomisation is smaller in diamonds, it means that the C-C bonds in diamond are weaker than in graphite because it requires less energy to change into the gaseous state.
Since diamond has more energy than graphite, there is a higher energy requirement to break the C-C bond to form new C=O bonds (in carbon dioxide) in combustion.
Q34. C) The electronegativity difference decreases between the elements (3.05, 2.13, 1.43, 0.65)
All of the compounds fulfill the octet rule and are isolelectronic.
The compounds become increasingly covalent (starting from ionic)
Q35. B) Sulphur dioxide is a reducing agent which prevents oxidation.
Since it's an anti-oxidant, it prevents alcohols from oxidizing to carboxylic acids (prevents sour-tasting acids).
It does smell and is toxic in large quantities.
Q36. C) Iodide ions are strong reducing agents and so they reduce the sulphuric acid, first to sulphur dioxide, then to sulphur and then hydrogen sulphide. Barely any hydrogen iodide is formed because it's displaced by the sulphuric acid.
Iodide ions are reducing agents, and become oxidised to iodine.
The majority of the products of the reaction are sulphur compounds (as explained above)
Q37. B) A chiral centre is an atom bonded to four different groups.
An optical isomer (geometric isomer) occurs when there's a chiral centre.
Chiral carbon atoms DO NOT need to have structural isomers.
Q38. B) Step X is a nucleophilic substitution because the reagent is hot aqueous sodium hydroxide (OH- being the nucleophile).
A chloroalkane cannot be formed by reacting sodium chloride with alcohol. It can be done with phosphorus (III) chloride or phosphorus (V) chloride.
Q39. C) Only an aldehyde forms a brick-red precipitate with Fehling's solution. Aldehydes are formed by the oxidation (in acidified dichromate) of primary alcohols. The two primary alcohols are CH3CH2CH2OH and CH3OH
Q40. B) It only has one chiral carbon (The one in the middle).
It has a carboxylic acid group, so it can be esterified by ethanol. It has an OH group, so it can be esterified by ethanoic acid.
The molecule contains tertiary and primary alcohols, not secondary.
JazakAllah khairan!! One small doubt, tho. In the autocatalysed reaction, yeah the conc. of reactant decreases, but the conc. of product doesn't right? so since the product is the catalyst here, shouldn't the graph become a horizontal line like that of B.
Ethyl ethanoate is not very soluble in water.http://papers.xtremepapers.com/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_w03_qp_1.pdf
Can anybody please explain question 30?
Why can't D be the answer as it also react with NaOH as hydrolysis happens?
No it is soluble I found that in another paper.Ethyl ethanoate is not very soluble in water.
Got it! Thanks!Notice that the Y-axis is measuring speed of reaction, not amount of products.
When the reactants gets used up towards the end, the speed of reaction drops back towards zero.
The decomposition temperature of CaCO3 is above 800 plus degrees Celsius if I remember correctly.
Well, I'm actually a teacher myself..
The decomposition temperature of CaCO3 is above 800 plus degrees Celsius if I remember correctly.
Time taken to reach that temperature? Well, it depends on how strongly its being heated?
This procedure that you are carrying out, is it based on the actual test question or is actually a self designed experiment?
number of moles of Tl+NO3-=10*0.30/1000View attachment 44145
Answer: B Howww?
No it is soluble I found that in another paper.
ohh ohokay, i never knew sir, sir its this that we are provided with Caco3 and Kcl mixture and have been provided with crucible and heating apparatus and some Hcl also, my teacher is saying that it must be something related to percenatage impurity or purity, so by the loss in mass we can deduce it, but whenever we are heating it it is not decomposing.... can u deduce any experiment with that? or help us out through this?
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