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Chemistry: Post your doubts here!

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http://studyguide.pk/Past Papers/CIE/International A And AS Level/9701 - Chemistry/9701_s08_qp_2.pdf
For question 5 part 3, it says F is heated with H2SO4. What I don't get is how does it change to a carboxylic acid when H2SO4 is used as a dehydrating agent? Or wait.. Only conc H2SO4 is dehydrating agent then wbu dilute? Plus for part e I know it should be an alcohol but can't be a carboxylic acid as Na also reacts with carboxylic acid to form H2? Someone HELP!
SOMONE FOR HEAVENS SAKE HELP ME THROUGH THIS CRAP.
 
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SOMONE FOR HEAVENS SAKE HELP ME THROUGH THIS CRAP.
It's known as acid hydrolysis, an organic nitrile compound + mineral acid= carboxylic acid.. Organic nitrile compound + NaOH(alkali)- Sodium salt of carboxylic acid.
Chapter- carboxylic acids and their derivatives.
The compound must be C2H2O2 as it's an isomer, it can't be an acid as the C would need 3 hydrogens and the MF will be C2H4O2..
 
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It's known as acid hydrolysis, an organic nitrile compound + mineral acid= carboxylic acid.. Organic nitrile compound + NaOH(alkali)- Sodium salt of carboxylic acid.
Chapter- carboxylic acids and their derivatives.
The compound must be C2H2O2 as it's an isomer, it can't be an acid as the C would need 3 hydrogens and the MF will be C2H4O2..
So, if it's an alcohol then it'll be C2(OH)H2 with double bond between C=C?
 
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http://studyguide.pk/Past Papers/CIE/International A And AS Level/9701 - Chemistry/9701_s08_qp_2.pdf
In this same paper part aii, why can't we write the structural formula like CO2H CO2H? why do we have to writeHO2CCO2H? I always get confused while writting structural formulas! :confused::mad: SOMEONE? :rolleyes::rolleyes:
If you're referring to this:
300w%5C2011-9%5C3278fb09-5d6f-4674-9699-37151c0a9f24.gif

Then we must write this as:
HO2CCO2H

Or as:
HOOCCOOH

We cannot however, put:
CO2HCO2H,
Since the carbons are bonded together, and in this you cannot tell that the carbons are bonding, rather it seems as though the carbon is bonded to hydrogen!
 
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Those lone pairs tho

You always seem to be panicking in your questions :p
A is with an alcohol so the malic acids Carboxy groups will react with them to form a diester
B is with a carboxylic acid so it'll react with the single OH present to form an ester.


Just keep these 2 things in mind and draw the structural formula like your simply making an ester from an acid and an alcohol.

Some of these questions arent that much of a problem,so i think you should at least revise the syllabus of organic a few times,and then attempt the past papers,no use just doing them without a clear concept.

Thanks! I did do that, but my structure was kinda messed up. :/

There are just sooooo many reactions and equations to remember. :'( I always forget one thing or the other. -_-

Thanks again though. :)
 
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Here's the mark scheme: http://freeexampapers.com/A-Level/Chemistry/CIE/2012-Jun/9701_s12_ms_22.pdf

My doubt: How do I figure out how many lone pairs are present?

Look at the groups in which Nitrogen and Sulfur reside.

Nitrogen is in group 5 and Sulfur in group 6.
That means Nitrogen has 5 electrons in its outer-shell, and Sulfur, 6.

The number of bonds an atom can form is,
No of bonds = Full valence shell - Number of valence electrons

For example, nitrogen already has 5 electrons, it needs 3 more to achieve a noble gas structure. So it will form 3 bonds.
The above formula works the same way,
No of bonds in N = 8 - 5 = 3

So with that in mind, Nitrogen can form 3 bonds and Sulfur can form 2.

The next thing to note, is that each bond will have two electrons.
Since nitrogen needs to form 3 bonds, it will need 6 electrons.
Sulfur needs to form 2 bonds, so it will need 4 electrons.

Out of the 8 electrons that can exist in the outer-shell,

-Nitrogen needs 6, which leaves 2 electrons not participating in any bond.
-Sulfur needs 4, which leaves 4 not participating in a bond.

A lone pair = 2 electrons not participating in a bond.

Nitrogen therefore has 1 lone pair and Sulfur has 2.

Hope that helped you! (y)
 
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Look at the groups in which Nitrogen and Sulfur reside.

Nitrogen is in group 5 and Sulfur in group 6.
That means Nitrogen has 5 electrons in its outer-shell, and Sulfur, 6.

The number of bonds an atom can form is,
No of bonds = Full valence shell - Number of valence electrons

For example, nitrogen already has 5 electrons, it needs 3 more to achieve a noble gas structure. So it will form 3 bonds.
The above formula works the same way,
No of bonds in N = 8 - 5 = 3

So with that in mind, Nitrogen can form 3 bonds and Sulfur can form 2.

The next thing to note, is that each bond will have two electrons.
Since nitrogen needs to form 3 bonds, it will need 6 electrons.
Sulfur needs to form 2 bonds, so it will need 4 electrons.

Out of the 8 electrons that can exist in the outer-shell,

-Nitrogen needs 6, which leaves 2 electrons not participating in any bond.
-Sulfur needs 4, which leaves 4 not participating in a bond.

A lone pair = 2 electrons not participating in a bond.

Nitrogen therefore has 1 lone pair and Sulfur has 2.

Hope that helped you! (y)

That really did help! Thank you!!
 
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Q.P: http://freeexampapers.com/A-Level/Chemistry/CIE/2013-Nov/9701_w13_qp_21.pdf
M.S : http://freeexampapers.com/A-Level/Chemistry/CIE/2013-Nov/9701_w13_qp_21.pdf

-In question 2b(ii) Do the isomers of the 3 Cyclic compounds represent cis-trans isomerism? If so, then how does cis-trans isomerism arise in cylclic compounds because I know that it occurs across double bonds of alkenes.

-And I really could not understand question 4(f).

It would be realy nice if someone could help.
And Thanks in Advance!
 
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Need help!!!

There's two axes, solvent 1 and solvent 2.

If the points move across the x axis, they have separated from solvent 2.
If the points move across the y axis, they have been separated from solvent 1.

It's asking for the "two" amino acids, that did not separate from solvent 1. Which means these two points are on the same line.
1430207429303.jpg

They did separate from solvent 2 though.
 
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Q.P: http://freeexampapers.com/A-Level/Chemistry/CIE/2013-Nov/9701_w13_qp_21.pdf
M.S : http://freeexampapers.com/A-Level/Chemistry/CIE/2013-Nov/9701_w13_qp_21.pdf

-In question 2b(ii) Do the isomers of the 3 Cyclic compounds represent cis-trans isomerism? If so, then how does cis-trans isomerism arise in cylclic compounds because I know that it occurs across double bonds of alkenes.

-And I really could not understand question 4(f).

It would be realy nice if someone could help.
And Thanks in Advance!

Cis/Trans isomerism is basically just geometrical isomerism. It does not only apply to alkenes only, but to cycloalkanes too. They both have the formula CnH2n.

Try to think of the cycloalkane, as a ring placed flat on a surface. There are two planes, the top and the bottom one. So when you substitute an atom in place of the hydrogen, it really matters whether the atom is on the top or bottom plane.

For cyclopropane, since you're adding 2 chlorine atoms, there's two possible options. The halogen atoms are on the same carbon, or on two different carbons. Once you've finished drawing the structure for the atoms being on the same carbon, you have to consider the other situation.

When they are on two different carbons, they can both be on the same plane, or one on each. Similar to alkenes, when they're on the same plane, they're cis, and on different planes, trans.

----------------------------

For 4(f), you're going to be using your answer to (e).

If you look at the formula of your isomer, it's C4H4O4. In (f), it's C4H2O3.
Water has been removed, since two hydrogen atoms and one oxygen atom have been removed from the formula.

Now for this to happen, the OH group at the end of both -COOH groups, need to be close to each other, in order for this to happen under the presence of heat.
If you use your trans isomer, the -CO(OH) endings are far apart when compared to cis, so that's why trans does not react at the that temperature. ( 110 degrees )

The way it works is, the OH groups being close to other, one of the carbons ejects its OH group completely. With the OH- ion now with a lone pair, it attracts the H on the other -COOH group.

You end up with a molecule as such,

-COCH=CHCOO-

One carbons missing a bond and on the other end, oxygen is missing a bond. So the two end up sharing a bond, forming the cyclic compound.

Screen Shot 2015-04-28 at 3.11.27 PM.png -------> Screen Shot 2015-04-28 at 3.12.26 PM.png --------> Screen Shot 2015-04-28 at 3.12.42 PM.png

Hope all of that made sense! (y)
 

NIM

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There's two axes, solvent 1 and solvent 2.

If the points move across the x axis, they have separated from solvent 2.
If the points move across the y axis, they have been separated from solvent 1.

It's asking for the "two" amino acids, that did not separate from solvent 1. Which means these two points are on the same line.
View attachment 52614

They did separate from solvent 2 though.
Can u plz tell me the third part as well!!
Thnx a lot for d help
 
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