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AS Chemistry- helping each other out!

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Original post by Amethyst-Wolf
Hey guys I'm stuck on this one question.

The fuel tank of one type of hydrogen-powered car holds 70kg of magnesiumhydride. Calculate the volume of hydrogen gas, measured at room temperature and pressure,which would be produced if this amount of magnesium hydride reacted with water.

MgH2(s) + 2H2O(I) -----> Mg(OH)2(s) + 2H2(g)


The marking scheme says this :

Moles MgH2 = 70000 = 2659.6 (2660) (1)

26.32Moles H2 = 5319.2 (5320) (1) I've gotten to here, but I just cant figure out what to do to get the next answer.

Volume H2 = 1.28 × 105dm3(1)


Thanks for any help!


The answer is expressed in index form. Your value should be somewhere around 128,000 dm3 in standard form. (1.28 * 10^5)

After you have correctly gotten the moles of H2(g) which is 5319.2 using mole ratio from equation and mol of MgH2 (from your periodic table). Multiply that value by the molar volume at room temperature and pressure (RTP) which is always 24 dm3. You should get: 127,660.8 dm3 which is close enough. You can round up to get 128,000dm3. You can multiply that by 1000 to convert to cm3 if you want.

So it's (mol of product) * 24 dm3 (Vm) = V
Thanks _NMcC_ ! Thats super helpful :smile:
Original post by RagaZ
Saw you guys were a bit confused... One of the above posters are right, Br2(aq) is bromine water, Br-OH? Nope

I've drawn the mechanism below and am pretty certain it's right, this stuff comes up in A2 too

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That's wrong. Bromine adds anti to a double bond

EDIT: it should be like this
(edited 8 years ago)
Anyone have got paper 2015


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Original post by annie79
when bromine water (Br-OH) is added to an alkene, is it the Br or OH that is the nucleophile in the mechanism for the reaction?


Original post by C0balt
Br2+H2O->BrOH+HBr

Posted from TSR Mobile


The Alkene is the nucleophile. The Alkene reacts with the Br-Br. How could BrOH even react? It would dissociate as BrO- and H+. And that equilibrium lies well to the left anyway.
Just a note: you'll lose marks if the curve arrow is not touching the bond
Original post by langlitz
The Alkene is the nucleophile. The Alkene reacts with the Br-Br. How could BrOH even react? It would dissociate as BrO- and H+. And that equilibrium lies well to the left anyway.


Well I don't have that much knowledge I'm afraid
I just remember my teacher saying bromoalcohol forms with bromine water because HOBr inside bromine water whatnot


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Original post by C0balt
Well I don't have that much knowledge I'm afraid
I just remember my teacher saying bromoalcohol forms with bromine water because HOBr inside bromine water whatnot


Posted from TSR Mobile


HoBr doesn't form. In AQ the bromine adds to one carbon of the double bond forming a carbocation as normal. The bromine is AQ so compared to the other nucleophile present (water) there is very little of the bromine - ions. Therefore the major product involves the water adding to the carbocation and then the extra hydrogen reacts with a lone pair from another water molecule forming an H3O (hydronium) ion

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Original post by langlitz
That's wrong. Bromine adds anti to a double bond

EDIT: it should be like this


This is A-level, it's a simplified version. What RagaZ drew is perfectly acceptable (at least for AQA)
Original post by samb1234
HoBr doesn't form. In AQ the bromine adds to one carbon of the double bond forming a carbocation as normal. The bromine is AQ so compared to the other nucleophile present (water) there is very little of the bromine - ions. Therefore the major product involves the water adding to the carbocation and then the extra hydrogen reacts with a lone pair from another water molecule forming an H3O (hydronium) ion

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thats makes more sense
teacher wtf
Reply 2530
resitting unit two even though I got 83/100 (which was just an A), to get a higher A.
Forgotten most of the content, so I'm starting my revision for this now :biggrin:
Original post by C0balt
thats makes more sense
teacher wtf


Yeah I found what you were talking about but there is definitely no BrOH involved
image.jpg
Original post by Dylann
This is A-level, it's a simplified version. What RagaZ drew is perfectly acceptable (at least for AQA)


Well it's wrong never the less. Pretty sure we did it in advanced higher
Original post by langlitz
Yeah I found what you were talking about but there is definitely no BrOH involved
image.jpg


Brb I'll go smack my teacher's head

Jk lol
Thanks anyway haha


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Reply 2534
I posted a thread earlier but does anyone want to study f322 with me? Over chat ( kik/Facebook etc ) haha

Id find it really helpful if we set an amount of work to do and then test one another, discuss past paper results etc

I need motivation and to have someone to discuss things with would really help

Would anyone be interested?

ps idm who but someone who is doing last minute revision etc, not someone who knows the whole spec already :tongue:

also for f324, if anyone is interested

Let me knowww
(edited 8 years ago)
Original post by langlitz
Well it's wrong never the less. Pretty sure we did it in advanced higher


No it's not "wrong" because it would get you the marks in an AS exam. Hey, look at the title of this thread, it says AS!! Not Advanced Highers!
Original post by Dylann
No it's not "wrong" because it would get you the marks in an AS exam. Hey, look at the title of this thread, it says AS!! Not Advanced Highers!


It is technically correct anyway as you will get some dibromoalkane formed but the major product would be a bromoalcohol

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Original post by NutE
resitting unit two even though I got 83/100 (which was just an A), to get a higher A.
Forgotten most of the content, so I'm starting my revision for this now :biggrin:


if the papers the same as last year uh oh :biggrin:. Or you could benefit from the low boundaries haha
Original post by samb1234
It is technically correct anyway as you will get some dibromoalkane formed but the major product would be a bromoalcohol

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No it's not 'technically correct'... both the bromoalcohol and dibromoalkane form via the bromonium ion intermediate.
Reply 2539
Original post by ThatGuyRik
if the papers the same as last year uh oh :biggrin:. Or you could benefit from the low boundaries haha


what do you mean? :smile:

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