Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Noob Getting Started in OC
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 9-4-2014 at 14:11
Noob Getting Started in OC


Any suggestions on where to get started in OC gratefully received.

In particular, is there a shortlist of reagents & kit required ?

To be clear : i'm not asking what stuff i need to build an elephant from scratch, just a list of stuff i will need to conduct the first reactions that you did when you got started, and what those reactions were.

Something achievable would be good !

Many thanks.
View user's profile View All Posts By User
Bert
Super Administrator
Thread Moved
9-4-2014 at 14:14
DraconicAcid
International Hazard
*****




Posts: 4334
Registered: 1-2-2013
Location: The tiniest college campus ever....
Member Is Offline

Mood: Semi-victorious.

[*] posted on 9-4-2014 at 14:24


That would depend on what you're trying to do in organic chemistry.

Most of the organic chemistry I have done was in classes, not at home, but you could probably do some esterification reactions. Start with aspirin, hydrolyze to salicylic acid, then make methyl salicylate from that. Mmmmmm...wintergreeny.

[Edited on 9-4-2014 by DraconicAcid]




Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
View user's profile View All Posts By User
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 9-4-2014 at 14:38


I will be trying to Understand something of organic chemistry.

There is no particular 'product' that i wish to produce.
View user's profile View All Posts By User
Random
International Hazard
*****




Posts: 1120
Registered: 7-5-2010
Location: In ur closet
Member Is Offline

Mood: Energetic

[*] posted on 9-4-2014 at 14:41


You will need to understand aliphatic series, aromatics and functional groups, after that reactions between functional groups and name reactions in organic chemistry for the beginning.
View user's profile View All Posts By User
Chemosynthesis
International Hazard
*****




Posts: 1071
Registered: 26-9-2013
Member Is Offline

Mood: No Mood

[*] posted on 9-4-2014 at 14:47


http://www.sciencemadness.org/talk/viewthread.php?tid=29979#...

Some books referenced here to get you started. Lab books for labs, lecture for more theory.
View user's profile View All Posts By User
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 9-4-2014 at 15:02


As i recall, that thread was full of flames, due to a grounded suspicion that the originator was a recipe kiddie looking for help to make stuff.

I will follow the links, so thanks for pointing out that the links are there.

It would be well if my intent were to be known : i wish to know something of organic chemistry, and am a beginner, rather than a chancer looking for the Gold from Lead recipe.
View user's profile View All Posts By User
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 9-4-2014 at 15:04


Quote: Originally posted by Random  
You will need to understand aliphatic series, aromatics and functional groups, after that reactions between functional groups and name reactions in organic chemistry for the beginning.


aliphatics
aromatics
functional groups

Thanks. Googling commenced ...

[Edited on 9-4-2014 by aga]
View user's profile View All Posts By User
blogfast25
International Hazard
*****




Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline

Mood: No Mood

[*] posted on 10-4-2014 at 05:31


Definitely esterifications, they're practically a 'rite of passage' for the beginning OC. Small esters are easy to make and different types have different 'fruity' aromas: apple, pear, pineapple, banana, 'cognac' etc etc. Only problem is that getting hold of the starting materials (the various acids and alcohols) isn't always that easy.

But glacial acetic acid and ethanol are easy enough to get (for ethyl acetate). Esterifications also offer good opportunities for work-up/distillation, so typical of OC...

[Edited on 10-4-2014 by blogfast25]




View user's profile View All Posts By User
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 10-4-2014 at 09:15


Esterificiations it is then.

Funny, but this bottle of vodka is going down quite fast ...
View user's profile View All Posts By User
blogfast25
International Hazard
*****




Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline

Mood: No Mood

[*] posted on 10-4-2014 at 09:19


Quote: Originally posted by aga  
Esterificiations it is then.

Funny, but this bottle of vodka is going down quite fast ...


You need pure ethanol (95 % or better) for esterifications. Of course you could distil your vodka. :)

Also pure acids (vinegar will do diddly squat) are needed. And 95 % or better H2SO4 as catalyst for Fisher esterifications.




View user's profile View All Posts By User
DraconicAcid
International Hazard
*****




Posts: 4334
Registered: 1-2-2013
Location: The tiniest college campus ever....
Member Is Offline

Mood: Semi-victorious.

[*] posted on 10-4-2014 at 09:25


Making ethyl acetate is rather dull (it doesn't smell particularly interesting). If you're making an ester for the sake of an ester, it's probably easier to get reasonably pure isopropyl alcohol than ethanol.



Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
View user's profile View All Posts By User
blogfast25
International Hazard
*****




Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline

Mood: No Mood

[*] posted on 10-4-2014 at 09:30


Quote: Originally posted by DraconicAcid  
Making ethyl acetate is rather dull (it doesn't smell particularly interesting). If you're making an ester for the sake of an ester, it's probably easier to get reasonably pure isopropyl alcohol than ethanol.


It smells of Velpon, the one time popular clear all purpose glue. Broken cars were glued back together with that, in desperation, back in those days! ;)




View user's profile View All Posts By User
ElizabethGreene
Hazard to Others
***




Posts: 141
Registered: 15-10-2012
Member Is Offline

Mood: No Mood

[*] posted on 10-4-2014 at 10:47


I enjoy the plant part of oChem more than the "add this nondescript powder to that foul smelling liquid" part. My vote would be to take some time brew and distill ethanol and acetic acid as first projects. Try extracting Salicylic acid and Limonene from their plant origins. Those are really fun for me and make up for the requisite memorization of large chunks of minutiae.

Perhaps you want to create your own feline army?
http://www.instructables.com/id/DIY-Kitty-Crack%3a--ultra-po...

If you want your wife really mad, try Syn-propanethial-S-oxide. It's the lachrymatory decomposition product from cutting onions. (Do not do this in the garage.).




My Journal has moved to http://clutteredlab.com
View user's profile Visit user's homepage View All Posts By User
vmelkon
National Hazard
****




Posts: 669
Registered: 25-11-2011
Location: Canada
Member Is Offline

Mood: autoerotic asphyxiation

[*] posted on 10-4-2014 at 12:20


You can find a few nice things on Youtube.
How to make benzene (decarboxylation) from sodium benzoate.
How to nitrate benzene (conc H2SO4 and con HNO3).
How to reduce p-nitrobenzene to p-aminobenzene (I think it was with conc HCl and iron powder).

How to oxidize toluene to benzoic acid.
Esterification reaction benzoic acid + methanol.
Esterification reaction benzoic acid + ethanol.

There are some things that are multistep and look complicated. Look at how to make luminol by Nurdrage on Youtube.




Signature ==== Is this my youtube page? https://www.youtube.com/watch?v=tA5PYtul5aU
We must attach the electrodes of knowledge to the nipples of ignorance and give a few good jolts.
Yes my evolutionary friends. We are all homos here.
View user's profile View All Posts By User
DraconicAcid
International Hazard
*****




Posts: 4334
Registered: 1-2-2013
Location: The tiniest college campus ever....
Member Is Offline

Mood: Semi-victorious.

[*] posted on 10-4-2014 at 12:25


Quote: Originally posted by vmelkon  
How to reduce p-nitrobenzene to p-aminobenzene (I think it was with conc HCl and iron powder).

No such thing. There's nitrobenzene and aniline, or p-nitrobenzoic acid and p-aminobenzoic acid, but no p-nitrobenzene. The "p" indicates that the two substituents on the ring are para to each other (i.e., in the 1 and 4 positions), but nitrobenzene only has one substituent on the ring.




Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
View user's profile View All Posts By User
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 10-4-2014 at 14:20


Wow !

Now i really have some reading to do !

Mostest thanks peeps.

Oh. I only drink beer.
The vodka is still going down, just not my gullet ;)
View user's profile View All Posts By User
aga
Forum Drunkard
*****




Posts: 7030
Registered: 25-3-2014
Member Is Offline


[*] posted on 10-4-2014 at 14:30


Quote: Originally posted by ElizabethGreene  

Perhaps you want to create your own feline army?


Just No.

4 cats are enough, and they arrived pretty fast with no Cat-a-List present.

Quote: Originally posted by ElizabethGreene  
If you want your wife really mad, try Syn-propanethial-S-oxide


She gets mad anyway, so there's no need to provoke her further !

Currently it's my chemistry obsession that's making her mad, so yes, preparing that would work.
View user's profile View All Posts By User

  Go To Top