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Reply 500
Original post by otrivine
Hi how are you :smile:


Benzene, is a cyclic hydrocarbon and contains only carbon and hydrogen only. It is a trigonal planar (molecule/structure) and bond angle around each carbon atom is 120. Benzene has 4 outer shells of electrons, three of these electrons are shared between a carbon atom and one of the hydrogen atom, this called sigma bond and is sited above and below the plane of the carbon (C-C) bond. The 4th outer shell of electron is the 2p orbital in which the p orbital overlaps and creates a region of high electron density. The benzene is delocalised as the electrons are shared between the 6 carbon atoms , through out the whole structure. Also, in benzene the c-c bond length is the same.


you got full marks,

what causes optical isomerism? [2]
Reply 501
Original post by Zzzyax
you got full marks,

what causes optical isomerism? [2]


ok thanks!


If a chiral carbon is present in which the carbon is attached to 4 different atoms/groups of atoms and also that the 2 images are non-superimposable images of each other.
Reply 502
Original post by AishaTara
got a feeling its going to be a killer paper :/


Do you mean that it will be hard?
Original post by otrivine
Do you mean that it will be hard?


after the nice jan paper, yeah :/
Reply 504
Original post by otrivine
ok thanks!


If a chiral carbon is present in which the carbon is attached to 4 different atoms/groups of atoms and also that the 2 images are non-superimposable images of each other.


excellent answer, worth 3, infact,

my turn!:tongue:
Reply 505
Original post by Zzzyax
excellent answer, worth 3, infact,

my turn!:tongue:


Thanks:smile:


Stage the reagents and conditions needed for going from 3-chloropropan-1-ol to 3-aminopropan-1-ol (3)
Reply 506
Original post by AishaTara
after the nice jan paper, yeah :/


Its better being slightly hard than having a grade boundary of 51/60 for an A!
Reply 507
Original post by otrivine
Thanks:smile:


Stage the reagents and conditions needed for going from 3-chloropropan-1-ol to 3-aminopropan-1-ol (3)


( excess) NH3, ethanol? is it gently heated or something?
Reply 508
Original post by Zzzyax
( excess) NH3, ethanol? is it gently heated or something?


yes well done!


Give 2 uses of polyesters (2)
Reply 509
Original post by AishaTara
got a feeling its going to be a killer paper :/


the jan f325 was quite hardcompared to previous f325 papers, so the f324 so be a little easier than previous, and dont forget, about the extra time, which might mean everything gets harder?
Reply 510
Original post by otrivine
yes well done!


Give 2 uses of polyesters (2)


clothes, plastics

1) what is the structural formula of a lactic acid monomer
Reply 511
Original post by Zzzyax
clothes, plastics

1) what is the structural formula of a lactic acid monomer


clothes is correct, not sure about plastics, I would put carpets.


2-hydroxpropanoic acid

HOCH(CH3)COOH
Reply 512
Original post by otrivine
clothes is correct, not sure about plastics, I would put carpets.


2-hydroxpropanoic acid

HOCH(CH3)COOH


conditions/reagents for hydrolysis of
1)polypeptides
2) polyesters
3)polyamides
Reply 513
Original post by Zzzyax
conditions/reagents for hydrolysis of
1)polypeptides
2) polyesters
3)polyamides


hydrolysis of polypeptides, conditions , add HCL(aq) and heat under reflux for24 hours 6 mol dm-3, also alternatively under alkaline conditions usually with NaOH(aq)


Hydrolysis of polyesters, addition of h2o/H+ , heat under reflux , alkaline conditions


hydrolysis of polyamides, addition of aqueous HCL/ H2O and heat under reflux or again under alkaline conditions
Reply 514
Original post by otrivine
hydrolysis of polypeptides, conditions , add HCL(aq) and heat under reflux for24 hours 6 mol dm-3, also alternatively under alkaline conditions usually with NaOH(aq)


Hydrolysis of polyesters, addition of h2o/H+ , heat under reflux , alkaline conditions


hydrolysis of polyamides, addition of aqueous HCL/ H2O and heat under reflux or again under alkaline conditions



correct, all of them can be done in acid or alkali conditions, water needs to be present always, water solvent
Reply 515
Original post by Zzzyax
correct, all of them can be done in acid or alkali conditions, water needs to be present always, water solvent


thanks

Define:zwitterion


Define:isoelectric point
Reply 516
Original post by otrivine
thanks

Define:zwitterion


Define:isoelectric point



dipolar ionic form of an alpha amino acid, contains both positive and negative charges which cancel out leaving no overall charge,

the pH level where the zwitterion exists
Reply 517
Original post by Zzzyax
dipolar ionic form of an alpha amino acid, contains both positive and negative charges which cancel out leaving no overall charge,

the pH level where the zwitterion exists


yep, very nice!


my turn
Reply 518
Original post by otrivine
yep, very nice!


my turn



whats the name of a fatty acid which is represented as 6:1(3) ?
Reply 519
Original post by Zzzyax
whats the name of a fatty acid which is represented as 6:1(3) ?


ok my method

6=number of carbon atoms
1= number of double bonds
3=is the the position of double bond

therefore,

hexan-3-oic acid

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