It’s taken a long time – late April through early May was hectic – but today I’m thrilled to finally announce the launch of the “Organic Chemistry Reagent Guide“, a guide designed especially for undergraduate students taking Org1/Org 2. It’s has pretty much all the reagents you need to know about, from Ag2O to Zn(Hg).
-a front section with extensive tables, including lists of acids, bases, oxidizing agents, reducing agents, reagents that add to aromatic rings, and organometallic reagents. Plus tables of common abbreviations, solvents, and pKas. There’s even a guide to Greek!
-a back section with profiles on over 80 reagents, including their structures, common names, reactions, and mechanisms
-a quick-reference index, with 2 pages of condensed information on every reagent covered in the book.

(Click here to download a PDF of the index)
- Accuracy is paramount for a document like this. I pay a bounty for typos and mistakes. If you buy the Guide, and tell me about any typos or mistakes you find – or have suggestions for things that have been omitted – I’ll send you a $5 reward through Paypal.
- You can use it risk free. If you are not completely satisfied that this is a useful guide for your course, I will give you a refund within 30 days of purchase.


masterorganicchemistry
com
{ 6 comments… read them below or add one }
Congrats!
Did you go through and color code all the atoms by hand in ChemDraw? That’d take up 95% of the time for me! Or did you have some shortcut way to color code the atoms?
I would color code the starting molecule, and then through cut/paste, the subsequent molecules would be color coded. But yes…. it was very time consuming. Looks nice though!
Nice work! This will be very useful.
Just FYI, there is a typo on you DIBAL page (example 3: “initially” is missing the 2nd “i”
fixed! thanks.
Interesting, but you might want have someone look over your files. I found some mistakes / confusion for example,
Structure of the isobutyl group is incorrect on the first pdf, which is actually of the secondary butyl.
Bs is not an abbr for the benznesulfonyl but the bromobenzenesulfonyl (abbreviating benzenesulfonyl as bOsyl just doesn’t make sense because there are no O’s between B and S)
fixed. Thanks for pointing this out.