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October 14, 2025, 05:01:32 pm

Author Topic: HSC Chemistry Question Thread  (Read 1294411 times)  Share 

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bdobrin

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Re: Chemistry Question Thread
« Reply #3165 on: November 08, 2017, 05:22:49 pm »
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Hi,

I was wondering if anyone could tell me what it means for a biopolymer to synthesize?

i.e. "douglas dennis was able to transfer genes from alcalegenes eutrophus that control PHB synthesis.

thanks,
ben

MisterNeo

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Re: Chemistry Question Thread
« Reply #3166 on: November 08, 2017, 10:33:44 pm »
+6
Hi,

I was wondering if anyone could tell me what it means for a biopolymer to synthesize?

i.e. "douglas dennis was able to transfer genes from alcalegenes eutrophus that control PHB synthesis.

thanks,
ben
It just means that the monomer units join together into a polymer. Synthesis is combining things, so in this instance it means the same as "polymerise".
would someone be able to illustrate using an example, how we use activity series to figure half equations of displacement redox stuff? thank you :)
Hey ;)
A redox reaction always has a species being oxidised (lose electrons) and a species being reduced (gain electrons). In a displacement reaction, you need to determine if the solid metal will oxidise and the cations reduce.
Let's say you placed a piece of zinc into copper nitrate in a displacement reaction.
Will the zinc oxidise? Will the copper ions reduce?
This is when the Data Sheet is your best friend.

The voltages are potentials, or how willing zinc is to lose electrons, or how willing copper is to gain electrons. The larger the potential, the more spontaneous the reaction is. To see if a displacement reaction will actually occur, you need to find the total potential (Eo value) by adding zinc's oxidation potential (0.76V) with copper ions reduction potential (0.34V), which is 1.1V. Since it is positive, a reaction will occur because the displacement is willing to occur (spontaneous). The above equations are your half-equations.
If the total potential were negative, such as copper metal in zinc ions, there would be no half-equations because nothing happens.
Hope this helps :)
Hey!
So I'm looking at the syllabus dot point which states Explain what is meant by a condensation polymer
I understand that a condensation polymer is a polymer (long chain molecule) formed when pairs of monomers join and a small molecule (usually water) is eliminated.
but I don't understand the statement "Condensation polymers are made from monomers that have two different groups of atoms that can join together"
*I put the bit I don't understand in bold
also, does
"One or two types of monomers can be involved and no double bond is required – the bond forms where the molecule is eliminated."
mean that there cannot be three monomers? Also does it also mean that alkanes can form condensation polymers?
I'm also not really sure what is being addressed in this statement
"The end product of condensation polymerisation depends on the number of functional end groups of the monomer that can react. If there is only one reactive group the growing chain will terminate. With two reactive end groups a linear polymer if formed. with three or more reactive end groups a three-dimensional, cross0-linked polymer can be made"

^This is a statement I have memorised, but I have no idea what it means. My main problem is that I don't understand/am not used to the terminology.
Esterification is a condensation reaction, but cannot polymerise because the 'monomers' only have one functional group each.

Cellulose is a condensation polymer because each glucose monomer has multiple functional groups.

For the 3D polymers, they're not in the syllabus. :P
Also, for the "describe condensation", you don't necessarily have to include where the water comes from. As long as you include "Monomers with two functional groups each polymerise to form a polymer and a small molecule such as water." then you'll get the marks. Give an example if you have enough lines, and talk about cellulose. :)
also how do we do q4 from the 2005 hsc
https://www.boardofstudies.nsw.edu.au/hsc_exams/hsc2005exams/pdf_doc/chemistry_05.pdf
The question states that the polymer is a condensation polymer, so the monomers must have two functional groups each (the two can be the same type). You can immediately eliminate A and C because of those H-benzene-H molecules, which have no functional groups (-H are not functional groups). All the other monomers have two hydroxyl groups that allow for condensation, however 1st one of Option B has a double bond, which would undergo addition on the carbons rather than condensation on its two hydroxyl groups. Hence, the answer is D. I would do a bit of trial-and-error tbh. ;D
can someone pls check my answers :/
CH3CHOHCH3
is that 2-propanol?

CH3CH2CHOHCH2CH2CH2OH
1,4-hex diol??
how do we draw this
Yep, they're both correct. :)
2-propanol can also be propan-2-ol
Admire my fabulous Paint skills...
« Last Edit: November 08, 2017, 10:53:29 pm by MisterNeo »

tina1395

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Re: Chemistry Question Thread
« Reply #3167 on: November 10, 2017, 08:33:38 pm »
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Hi,

For my assessment task we have to research an Australian practising chemist. I decided to write about Maria Skyllas-Kazacos, who is an electrochemist and pioneered the Vanadium Redox Battery. However, most of her work was done in the 1980/90s, and there isnt too much information about what she is doing now. Would she still be considered as a practising chemist if she has retired?

Thanks :)

itsangiej101

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Re: Chemistry Question Thread
« Reply #3168 on: November 12, 2017, 04:07:35 pm »
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Hey I have a chemistry research portfolio I have to finish and revise for an exam in like three days. Almost done but I have a section I'm not quite sure about

2.   There are three main processes involved for the industrial production of ethanol; filtering, fermentation and distillation. For each process answer the following;
i)   Physical or chemical reaction involved?
ii)   Why is this procedure used?
iii)   Outline the procedure.

This section is worth 3 marks
Any help is appreciated


daniel.hu3

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Re: Chemistry Question Thread
« Reply #3169 on: November 13, 2017, 11:05:26 am »
+3
Hey I have a chemistry research portfolio I have to finish and revise for an exam in like three days. Almost done but I have a section I'm not quite sure about

2.   There are three main processes involved for the industrial production of ethanol; filtering, fermentation and distillation. For each process answer the following;
i)   Physical or chemical reaction involved?
ii)   Why is this procedure used?
iii)   Outline the procedure.

This section is worth 3 marks
Any help is appreciated




I'll attempt to make this as concise as possible since this is a 3 mark question.

FILTERING (physical reaction): Before fermentation occurs, the sugar cane needs to be processed after it has been grown, harvested and transported. You are left with two main products- sugar and molasses. The high sucrose sugar cane juices are extracted via crushing. Sucrose is crystallised out and refined into table sugar. Molasses, a thick syrupy liquid still containing significant amounts of sucrose remains. Molasses is usually separated from the sugar by centrifuging, as it is denser than sugar, it falls to the bottom.

FERMENTATION (chemical reaction): The glucose molasses is fermented anaerobically by yeast to produce ethanol and carbon dioxide.(would be a good idea to include the fermentation equation here)
Conditions under which this reaction occurs: warm temperature of 37 degrees, anaerobic, presence of yeast, containing zymase enzymes, alcohol concentration of less than 15% v/v

DISTILLATION (physical reaction): The ethanol then undergoes distillation to produce purer ethanol of 95% v/v (this procedure is just to ensure you have ethanol of higher purity- additional info: afterwards, ethanol is also dehydrated to obtain 99.7% v/v, even higher purity!)

Please correct me if i made any mistakes, and hopefully this helps!

D.H.




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itsangiej101

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Re: Chemistry Question Thread
« Reply #3170 on: November 13, 2017, 01:08:34 pm »
0

I'll attempt to make this as concise as possible since this is a 3 mark question.

FILTERING (physical reaction): Before fermentation occurs, the sugar cane needs to be processed after it has been grown, harvested and transported. You are left with two main products- sugar and molasses. The high sucrose sugar cane juices are extracted via crushing. Sucrose is crystallised out and refined into table sugar. Molasses, a thick syrupy liquid still containing significant amounts of sucrose remains. Molasses is usually separated from the sugar by centrifuging, as it is denser than sugar, it falls to the bottom.

FERMENTATION (chemical reaction): The glucose molasses is fermented anaerobically by yeast to produce ethanol and carbon dioxide.(would be a good idea to include the fermentation equation here)
Conditions under which this reaction occurs: warm temperature of 37 degrees, anaerobic, presence of yeast, containing zymase enzymes, alcohol concentration of less than 15% v/v

DISTILLATION (physical reaction): The ethanol then undergoes distillation to produce purer ethanol of 95% v/v (this procedure is just to ensure you have ethanol of higher purity- additional info: afterwards, ethanol is also dehydrated to obtain 99.7% v/v, even higher purity!)

Please correct me if i made any mistakes, and hopefully this helps!

D.H.

Thank you so much daniel! I think the information you put up would be consise enough for the marks allocated

jakesilove

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Re: Chemistry Question Thread
« Reply #3171 on: November 13, 2017, 01:39:59 pm »
+2
Hi,

For my assessment task we have to research an Australian practising chemist. I decided to write about Maria Skyllas-Kazacos, who is an electrochemist and pioneered the Vanadium Redox Battery. However, most of her work was done in the 1980/90s, and there isnt too much information about what she is doing now. Would she still be considered as a practising chemist if she has retired?

Thanks :)

Hey!

I would probably recommend using a chemist that is currently working in some field in Australia. Not that you'll ever be assessed on this particular dot-point, but I believe the chemist ought to be 'practising'; Maria probably doesn't count as practising anymore.
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itsangiej101

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Re: Chemistry Question Thread
« Reply #3172 on: November 13, 2017, 07:54:17 pm »
0
I have an exam on wednesday thats both prac and research based. Does anyone know specifically what kind of questions exams usually ask relating to ethanol as fuel, production of ethanol (fermenation), comparison of battery cells and galvanic cell experiment?
Thanks!

MisterNeo

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Re: Chemistry Question Thread
« Reply #3173 on: November 13, 2017, 10:25:12 pm »
+1
I have an exam on wednesday thats both prac and research based. Does anyone know specifically what kind of questions exams usually ask relating to ethanol as fuel, production of ethanol (fermenation), comparison of battery cells and galvanic cell experiment?
Thanks!
Hey :)
From the top of my head, possible questions include:
-Calculate the mass of X produced if Y was used, sometime it gives you a graph to extract data. (Fermentation)
-Outline the conditions of fermentation and its limitations (the ethanol concentration).
-Advantages and disadvantages of ethanol as a alternative to octane fuel, environmentally and societal.
-Calculate X if this mass of ethanol was burned. This would involve heat of combustion and some variable of the -mCΔT formula, ie they might give you everything except mass of water and then ask you to calculate mass of water based on ethanol’s HoC.
-Battery cell questions are mostly always “Compare the impact in society and the environment...” which you would compare two batteries.
-Galvanic cell questions can give you two metals and ask you to draw a galvanic cell with the electrodes labelled (Data Sheet). Then they can ask you to write half equations/net ionic equation and calculate total E value. Also you may be asked to justify the use of a salt bridge.
Hope this helps, good luck with your exam ;)

mxrylyn

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Re: Chemistry Question Thread
« Reply #3174 on: November 15, 2017, 06:07:05 am »
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Hey.

I'm very confused about the  temperature In which ethanol gets dehydrated.

My chemistry contexts 2nd edition textbook says it happens at 350 degrees, but my Atarnotes chemistry poster says it happens at 170 degrees.

For the hydration of ethylene, my the aforementioned text bok says it happens at 300 degrees, but my Excel chem study guide says it happens at 70-100 degrees

justwannawish

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Re: Chemistry Question Thread
« Reply #3175 on: November 15, 2017, 07:04:07 pm »
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Hey guys,

Any advice on practicals about titration, dilutions and indicator testing?

MisterNeo

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Re: Chemistry Question Thread
« Reply #3176 on: November 15, 2017, 08:02:03 pm »
+4
Hey.

I'm very confused about the  temperature In which ethanol gets dehydrated.

My chemistry contexts 2nd edition textbook says it happens at 350 degrees, but my Atarnotes chemistry poster says it happens at 170 degrees.

For the hydration of ethylene, my the aforementioned text bok says it happens at 300 degrees, but my Excel chem study guide says it happens at 70-100 degrees
I’ve always used 300 for hydration and 170 for dehydration without any issues. :)
Hey guys,

Any advice on practicals about titration, dilutions and indicator testing?
An error I once made in titration was not reading the miniscus properly. Make sure it is read from the bottom of the concave at eye level. Don’t force out the liquid at the tip of the pipette because it has been calibrated to account for the lost volume. Rinse everything with the solution that is going to be used in it except for the conical flask (water). Don’t use a beaker to measure volume in titrations because its markings are estimated, use that tall beaker. Do the titration on top of a white surface like paper so that changes of the indicator colour are easier to see. Don’t put too much indicator (I did this lol) because they can skew the titration results if you overdo it as they’re slightly acidic/basic themselves. When the titration is approaching the end point, open the burette drop by drop and swirl the flask after every drop. If the drop of titre is clinging onto the top of the burette, don’t risk opening the burette anymore because you might end up adding multiple drops, which could exceed the end point. Instead, spray the droplet off with distilled water from one of those plastic bottles with the long tube. It doesn’t matter if concentration of the conical flask changes because the moles are still the same. The end point is reached when the colour change stays when you swirl the beaker. For example, titration NaOH with a weak acid you would use phenolphthalein. When the phenolphthalein keeps a slight pink shade even after you swirl the flask, that would be the end point.
Hope this helps ;)
« Last Edit: November 15, 2017, 08:04:48 pm by MisterNeo »

LaraC

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Re: Chemistry Question Thread
« Reply #3177 on: November 15, 2017, 08:10:45 pm »
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 Hello,

Sorry I'm new on this site so hope I'm not messing things round - not really sure how everything works yet! But Jake, you seem like the person I need to talk to atm!  ;) Getting rather confused about a few things in my HSC chemistry......
Wondering if you could help me with the following qu:
Carbowax can also be considered as an addition polymer of ethylene oxide {as well asn a condensation polymer formed from ethylene glycol} . Explain how this can be so.

Thanks so much!!

MisterNeo

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Re: Chemistry Question Thread
« Reply #3178 on: November 16, 2017, 12:36:03 am »
+2
Hello,

Sorry I'm new on this site so hope I'm not messing things round - not really sure how everything works yet! But Jake, you seem like the person I need to talk to atm!  ;) Getting rather confused about a few things in my HSC chemistry......
Wondering if you could help me with the following qu:
Carbowax can also be considered as an addition polymer of ethylene oxide {as well asn a condensation polymer formed from ethylene glycol} . Explain how this can be so.

Thanks so much!!

Hey! Welcome to ATAR Notes! ;)
An addition polymerisation occurs when monomers join to form a polymer and nothing else. This usually occurs when some part of the monomer is quite reactive or unstable. The pyramid-looking oxygen in ethylene oxide is quite unstable and will break. This also occurs in ethylene when forming polyethylene because the double bond is reactive.

A condensation polymerisation forms a small molecule along with the polymer, which is usually water. This occurs when the monomer itself is fairly stable but it has two functional groups (in this case, hydroxyl) that can break off to form the small water molecule. Ethylene glycol has those two -OH groups that allow condensation reactions to occur. The free radicals of the detached atoms then join together to form the carbowax polymer.

Hope this helps :)
« Last Edit: November 16, 2017, 12:40:13 am by MisterNeo »

LaraC

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Re: Chemistry Question Thread
« Reply #3179 on: November 16, 2017, 09:38:43 am »
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Thanks so much MisterNeo! That's great!  :D