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November 01, 2025, 11:38:55 am

Author Topic: Chemistry 3/4 2013 Thread  (Read 448755 times)  Share 

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lzxnl

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Re: Chemistry 3/4 2013 Thread
« Reply #915 on: June 05, 2013, 04:04:25 pm »
+2
Isotopes found can encompass all isotopes in existence...it's just that some are more common than others. That's why you rarely see carbon-13 for instance. However, as bromine 79 and bromine 81 are almost just as common, they will both contribute significantly to the mass spectrum.

The linkage holding the DNA backbone together is a covalent bond between a phosphate group and deoxyribose and looks like an ether linkage, although given the P=O bond, it's known as a phosphoester.
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Re: Chemistry 3/4 2013 Thread
« Reply #916 on: June 05, 2013, 06:13:04 pm »
0
Isotopes found can encompass all isotopes in existence...it's just that some are more common than others. That's why you rarely see carbon-13 for instance. However, as bromine 79 and bromine 81 are almost just as common, they will both contribute significantly to the mass spectrum.

The linkage holding the DNA backbone together is a covalent bond between a phosphate group and deoxyribose and looks like an ether linkage, although given the P=O bond, it's known as a phosphoester.

Almost; some possible isotopes would not be found naturally as they would decay really quickly.
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Re: Chemistry 3/4 2013 Thread
« Reply #917 on: June 05, 2013, 07:06:29 pm »
0
Hey there,

How would I name the ester HCOOCH(CH3)2?
I saw it in a STAV exam and was just wondering.

Thanks again beautiful people. ;)

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Re: Chemistry 3/4 2013 Thread
« Reply #918 on: June 05, 2013, 07:32:52 pm »
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Hey there,

How would I name the ester HCOOCH(CH3)2?
I saw it in a STAV exam and was just wondering.

Thanks again beautiful people. ;)
that looks like 2-propyl methanoate, I could be wrong though

So, (I think) we're reacting 2-propanol and methanoic acid. When naming the ester, the alcohol part is 2-propanol - CH3CH(OH)CH3
and the acid part is methanoic acid- HCOOH, once they have reacted and a water molecule is lost, you are left with HCOOCH(CH3)2

Sorry for the poor explanation :/
« Last Edit: June 05, 2013, 07:53:38 pm by eclipse »
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lzxnl

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Re: Chemistry 3/4 2013 Thread
« Reply #919 on: June 05, 2013, 08:09:23 pm »
+1
Think methyl methanoate. On the methyl part of the ester, remove two hydrogens and replace them with methyl groups.
You'd actually have 1-methylethyl methanoate. The 1-methylethyl means the ethyl group has a methyl group on carbon 1.
It is also known as isopropyl methanoate.
Although the reactions are correct.
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Re: Chemistry 3/4 2013 Thread
« Reply #920 on: June 05, 2013, 08:12:30 pm »
0
Think methyl methanoate. On the methyl part of the ester, remove two hydrogens and replace them with methyl groups.
You'd actually have 1-methylethyl methanoate. The 1-methylethyl means the ethyl group has a methyl group on carbon 1.
It is also known as isopropyl methanoate.
Although the reactions are correct.
ah, I stand corrected. Thank you :)
are you referring to the reaction between 2-propanol and methanoic acid? Is that one correct?
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Re: Chemistry 3/4 2013 Thread
« Reply #921 on: June 05, 2013, 08:55:00 pm »
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Yes, that reaction.
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Re: Chemistry 3/4 2013 Thread
« Reply #922 on: June 06, 2013, 02:28:40 pm »
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It should be 2-propyl methanoate
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lzxnl

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Re: Chemistry 3/4 2013 Thread
« Reply #923 on: June 06, 2013, 03:56:23 pm »
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http://en.wikipedia.org/wiki/Isopropyl_acetate
For the acetate/ethanoate, both names are fine apparently.
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Re: Chemistry 3/4 2013 Thread
« Reply #924 on: June 06, 2013, 06:09:07 pm »
+1
Hey, I did a practice exam today, and one of the questions was what are 2 functional groups found in a lipid.
In my mind I envisioned a glycerol molecule bound to three fatty acid chains via an ester bond, and I was a bit stuck because I was like ok there's ester bond functional group, but where's another? So I settled for alkane and alkene functional groups (if unsaturated) but I'm not really sure. I totally understand IF it was glycerol you could say hydroxyl coz it's a tri-ol and for the fatty acid chain carboxyl, but in the case of a lipid, they've been merged so there's an ester bond haha, I was confused!
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thushan

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Re: Chemistry 3/4 2013 Thread
« Reply #925 on: June 06, 2013, 10:14:15 pm »
+1
Hey, I did a practice exam today, and one of the questions was what are 2 functional groups found in a lipid.
In my mind I envisioned a glycerol molecule bound to three fatty acid chains via an ester bond, and I was a bit stuck because I was like ok there's ester bond functional group, but where's another? So I settled for alkane and alkene functional groups (if unsaturated) but I'm not really sure. I totally understand IF it was glycerol you could say hydroxyl coz it's a tri-ol and for the fatty acid chain carboxyl, but in the case of a lipid, they've been merged so there's an ester bond haha, I was confused!

Alkyl functional group...that's stretching it. Technically it is one...but I'm unsure as to whether they'd pay it.
Alkenyl functional group they should pay - it was paid on the VCAA exam once iirc.

Btw - there is an 'ester' functional group too.
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Re: Chemistry 3/4 2013 Thread
« Reply #926 on: June 07, 2013, 08:08:21 pm »
0
Hii guyss!:)
I was just having trouble deciphering what the question(VCAA 2002)  was asking ? I dont understand VCAA's assessment report comment , "Solvent, Stanozolol" and how only "one peak " is formed.

A pure substance was suspected of being the high molecular weight anabolic steroid Stanozolol. A sample
of this substance was dissolved in a suitable pure solvent and injected into a gas chromatograph. How
many peaks would you expect to see in the resulting chromatogram? Justify your result.

Thanks so much !! :)
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Re: Chemistry 3/4 2013 Thread
« Reply #927 on: June 07, 2013, 08:23:31 pm »
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Hii guyss!:)
I was just having trouble deciphering what the question(VCAA 2002)  was asking ? I dont understand VCAA's assessment report comment , "Solvent, Stanozolol" and how only "one peak " is formed.

A pure substance was suspected of being the high molecular weight anabolic steroid Stanozolol. A sample
of this substance was dissolved in a suitable pure solvent and injected into a gas chromatograph. How
many peaks would you expect to see in the resulting chromatogram? Justify your result.

Thanks so much !! :)

you might have misinterpreted the report. if the pure substance was dissolved in a suitable solvent before being injected into the gas chromatograph, two peaks would register, one due to the pure substance and one due to the solvent. (i think this is what 'solvent, stanozolol' is supposed to mean. perhaps 1 mark/2 marks was awarded to students who wrote that only one peak would be observed.
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Re: Chemistry 3/4 2013 Thread
« Reply #928 on: June 07, 2013, 09:09:43 pm »
0
What do you guys read from this? If there's a double-stranded section of DNA 100bp long, aka contains 200 nucleotides in total, you know 38% is G, therefore 38% is C, 12% T/A. One of the stranded contains 25 guanine bases, how many cytosine bases would be on the same strand? I got 51, tell me what you think it is, I basically said hmm, well 0.38*200 = 76 bases in total, yet on this strand there's only 25 thus 51 on the other strand, 51 on the other strand of G would mean 51 of C on the strand in question, yes?  :o
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Re: Chemistry 3/4 2013 Thread
« Reply #929 on: June 07, 2013, 10:29:52 pm »
+1
76 Gs in total - 25 on Strand 1, hence 51 on Strand 2; hence, 51 Cs on Strand 1.
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