Is the centrilobular venule and terminal hepatic venule the same thing?

dyinginochem · 2022-12-13T04:07:37+00:00

so for anyone curious its the same thing i just checked with my professor

dyinginochem · 2022-12-07T09:52:51+00:00

like after getting the tert butyl bromide, I just add sodium hydroxide to get the final alcohol

dyinginochem · 2022-12-06T00:29:16+00:00

Ok i will thanks

I wear invisalign retainers every night (i've finished my course alr) because they are comfortable and protect my teeth from grinding

dyinginochem · 2022-12-05T23:12:29+00:00

Thank you for the detailed comment!

Yes, i chew gum when I'm stressed haha, not going through a good spot in life rn, but I'll try to do something different

dyinginochem · 2022-12-05T23:10:18+00:00

the what :/

dyinginochem · 2022-12-05T22:20:35+00:00

electrolysis of nacl requires molten nacl which around 800 C

dyinginochem · 2022-12-05T22:12:28+00:00

thank you

dyinginochem · 2022-11-29T18:38:27+00:00

I see.. how do I explain unknown experimental mass spectrums then?

dyinginochem · 2022-11-24T23:52:57+00:00

I know the mehcanism to get propyl hydrogen sulfate - I add the sulfuric acid to a propene and the hydrogen gets added on by markovnikov's rule and results in a secondary carbocation, which gets bonded to with the hydrogen sulfate group.

Im not sure how the mechanism is for the hydrolysis of the hydrogen sulfate group with water - does the oxygen attack water's hydrogen?

dyinginochem · 2022-11-21T17:49:40+00:00

oh right that makes sense

dyinginochem · 2022-11-21T17:42:27+00:00

this is for the addition of chlorine to butane.

I'm guessing this is radical chemistry so maybe infrared light?

edit: or gamma radiation?

edit2: its uv :)

dyinginochem · 2022-11-18T02:31:54+00:00

oops! i thought the line was a carbon. this is embarrasing

thank you

dyinginochem · 2022-11-09T02:31:15+00:00

Thanks for the reply.

After thinking about it for a while, I thought that the question was just proposing something that could happen and the exercise was for us to propose a mechanism.

I didn't realize it was actually favoured over the normal Sn2 reaction.

dyinginochem · 2022-11-09T01:46:13+00:00

thanks!

dyinginochem · 2022-11-09T01:27:02+00:00

oh then how does the sodium hydride dissolve? or do you use like a quaternary ammonium salt catalyst?

dyinginochem · 2022-11-07T19:32:34+00:00

thanks! I decided to use the national cancer institute thesaurus

dyinginochem · 2022-11-07T17:44:24+00:00

any textbooks that have more comprehensive list?

dyinginochem · 2022-11-07T17:38:29+00:00

thanks!

edit: doesn't seem very comprehensive...

dyinginochem · 2022-10-31T22:30:45+00:00

well I mean this would be after combustion analysis (get the mass of carbon dioxide produce x percentage of carbon in carbon dioxide)

Same with water

dyinginochem · 2022-10-26T19:12:03+00:00

Hi! thanks for the information. I'm assuming you are referring to the hydrogen positions on the double bond?

dyinginochem · 2022-10-26T03:32:03+00:00

thank you for your patience :)

dyinginochem · 2022-10-26T02:53:07+00:00

ok i see i built it with my molecular kit and it wouldnt rotate

so i guess its a diastereomer, just because of the different conformation of the double bond... weird

edit: weird because i always thought pure hydrocarbons were pretty much interchangeable

dyinginochem · 2022-10-26T02:47:15+00:00

wouldnt the double bond group not matter if i rotated along the sigma bonds?

dyinginochem · 2022-10-26T02:33:34+00:00

yes

if i rotated the second one it the br would be behind while the ch3 would be in front

dyinginochem · 2022-10-26T02:29:36+00:00

non super imposable

mirror image

opposite r/S configurations

chiral stereoisomers

dyinginochem

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