ATAR Notes: Forum
VCE Stuff => VCE Science => VCE Mathematics/Science/Technology => VCE Subjects + Help => VCE Chemistry => Topic started by: RobM8 on June 04, 2011, 03:35:35 pm
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Distinction between esterification and transesterification?
I have only seen the sates of the carboxylic acid, the alcohol and the resulting ester as (l), would you be incorrect to put the states of the produced ester, and the reacted carboxylic acid and alcohol as (aq) ?
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It would be ok to write the carb acid and alcohol as aqueous, but not the ester.
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Esterification = Forming an Ester between a Carboxyl and an Alkanol, emitting water in the process
Trans = Swapping one ester with another, ie triglyceride -> 3x methyl esters.
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Thanks lads
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It would be ok to write the carb acid and alcohol as aqueous, but not the ester.
That is not correct.
Esterification does not occur in the presence of water; you cannot label the carboxylic acid or the alkanol as aqueous. This is not a reaction in aqueous solution, even though water may be *produced* by it.
The carboxylic acid, alkanol and ester would all be either (l) or (s).
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It would be ok to write the carb acid and alcohol as aqueous, but not the ester.
That is not correct.
Esterification does not occur in the presence of water; you cannot label the carboxylic acid or the alkanol as aqueous. This is not a reaction in aqueous solution, even though water may be *produced* by it.
The carboxylic acid, alkanol and ester would all be either (l) or (s).
Hmm. So if we had:
Ethanoic acid and ethanol, we would make the liquids and the product (ester) a liquid also even though water is 'produced' in the course?
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It would be ok to write the carb acid and alcohol as aqueous, but not the ester.
That is not correct.
Esterification does not occur in the presence of water; you cannot label the carboxylic acid or the alkanol as aqueous. This is not a reaction in aqueous solution, even though water may be *produced* by it.
The carboxylic acid, alkanol and ester would all be either (l) or (s).
Hmm. So if we had:
Ethanoic acid and ethanol, we would make the liquids and the product (ester) a liquid also even though water is 'produced' in the course?
Yes that's right :)
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It would be ok to write the carb acid and alcohol as aqueous, but not the ester.
That is not correct.
Esterification does not occur in the presence of water; you cannot label the carboxylic acid or the alkanol as aqueous. This is not a reaction in aqueous solution, even though water may be *produced* by it.
The carboxylic acid, alkanol and ester would all be either (l) or (s).
Hmm. So if we had:
Ethanoic acid and ethanol, we would make the liquids and the product (ester) a liquid also even though water is 'produced' in the course?
Remember H2SO4 catalyst is also liquid, got marked down for writing (aq)
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Is there any general rules with writing states? Usually I just guess... ???
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Is there any general rules with writing states? Usually I just guess... ???
Amen to that hahaha
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Is there any general rules with writing states? Usually I just guess... ???
For the reaction pathways, learn them.
Otherwise, use your knowledge of the molecules' properties to help you guess :)
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Is there any general rules with writing states? Usually I just guess... ???
For the reaction pathways, learn them.
Otherwise, use your knowledge of the molecules' properties to help you guess :)
This, but as a general rule when anything is in the presence of water use H2O as a liquid and anything else as aq. Otherwise, know your precipitates in reactions, like AgCl and PbEverything.
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Alcohol and carb acid MUST be in liquid state. So is the ester. Otehrwise - no marks.
Chem Teacher.
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Is there any general rules with writing states? Usually I just guess... ???
For the reaction pathways, learn them.
Otherwise, use your knowledge of the molecules' properties to help you guess :)
This, but as a general rule when anything is in the presence of water use H2O as a liquid and anything else as aq. Otherwise, know your precipitates in reactions, like AgCl and PbEverything.
yeah this general rule is not great... see rena-bena's post...
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Okay, can we maybe just write some general rules down for these sorts of things.
Combustion:
Alkane(g) + O2(g) --> CO2(g) + H2O(g)
Esterification:
Alkanol (l) + Carboxylic Acid (l) - H2SO4(l) -> Ester (l) + H2O(l)
Hydrogenation:
Alkene(g) + H2(g) - Ni -> Alkane(g)
Halogenation:
Alkane(g) + Cl2(g) - UV Light -> Chloroalkane(g) + HCl(g)
Alkanol(aq) - PCl5 -> Chloroalkane(g)
Chloroalkane(g) - NaOH(aq) -> Alkanol(g) + NaCl(g)
Alkanol(aq) - Cr2O72-(aq) / H+(aq) -> Carboxylic Acid(aq)
Alkene(g) + H2O(g) - H3PO4(aq) -> Alkanol(aq)
Feel free to clean up any of the ones I have mentioned, but that's what I've got in my notes...
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NaCl gas?
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NaCl gas?
Hahaha, I was just writing out what was on my summary sheet. I'll change that, but what about the rest?
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Okay, can we maybe just write some general rules down for these sorts of things.
Combustion:
Alkane(g) + O2(g) --> CO2(g) + H2O(g)
Esterification:
Alkanol (l) + Carboxylic Acid (l) - H2SO4(l) -> Ester (l) + H2O(l)
Hydrogenation:
Alkene(g) + H2(g) - Ni -> Alkane(g)
Halogenation:
Alkane(g) + Cl2(g) - UV Light -> Chloroalkane(g) + HCl(g)
Alkanol(aq) - PCl5 -> Chloroalkane(g)
Chloroalkane(g) - NaOH(aq) -> Alkanol(g) + NaCl(g)
Alkanol(aq) - Cr2O72-(aq) / H+(aq) -> Carboxylic Acid(aq)
Alkene(g) + H2O(g) - H3PO4(aq) -> Alkanol(aq)
Feel free to clean up any of the ones I have mentioned, but that's what I've got in my notes...
Nice.
Does alkene (g) and steam go to alkanol (aq)?
Could some please confirm the aqueous part?
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Okay, can we maybe just write some general rules down for these sorts of things.
Combustion:
Alkane(g) + O2(g) --> CO2(g) + H2O(g)
Esterification:
Alkanol (l) + Carboxylic Acid (l) - H2SO4(l) -> Ester (l) + H2O(l)
Hydrogenation:
Alkene(g) + H2(g) - Ni -> Alkane(g)
Halogenation:
Alkane(g) + Cl2(g) - UV Light -> Chloroalkane(g) + HCl(g)
Alkanol(aq) - PCl5 -> Chloroalkane(g)
Chloroalkane(g) - NaOH(aq) -> Alkanol(g) + NaCl(g)
Alkanol(aq) - Cr2O72-(aq) / H+(aq) -> Carboxylic Acid(aq)
Alkene(g) + H2O(g) - H3PO4(aq) -> Alkanol(aq)
Feel free to clean up any of the ones I have mentioned, but that's what I've got in my notes...
Nice.
Does alkene (g) and steam go to alkanol (aq)?
Could some please confirm the aqueous part?
depends entirely on the length of the alkanol - short ones would be aq and longer ones liquid.
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is this why they have the states in the data book?
Also, is it just better we know whether it's aq/l (hence polar/non-polar) as opposed to whether it's gaseous?