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Use this tag for questions relating to organic molecules and their properties (structure of organic molecules, spectroscopic properties, reaction mechanisms, stereochemistry etc). DO NOT use this tag as the only tag in your question, as this tag by itself cannot appropriately classify your question. Always use this tag in addition to other more specific tags.
3
votes
Do I need a license or certificate to practice chemistry or what are the advantages if did h...
Over here, that is Germany, you will hardly find a job in chemical industry or academia without an academic degree (B.Sc., M.Sc, Ph.D) or a formal technical education (typically three years).
Most su …
4
votes
Accepted
Why is the decarboxylation of 2-hydroxybenzoic acid (and related compounds) done 'under nitr...
[…] it seems even more important to get the right mixture of gases around it at 122℃
No, it's only important to keep the oxygen away while you are heating the sample.
Have a look at the structur …
1
vote
Organic reactions reactions memorising
Recognize functional groups.
Be aware what nucleophiles and electrophiles are.
Apply 2 on 1.
Yes, there's more to it, and you still have to memorize name reactions, but the upper will definitely ma …
2
votes
Accepted
Process to separate Lauric Acid from Coconut Oil
With respect to economy, waste management and regulations concerning food processing, your current approach, a solvent-free crystallization, is probably the most reasonable approach.
There's a Unilev …
4
votes
Regioselectivity in radical chlorination of a carboxylic acid
Yes, we can :-D
Note the $h\nu$ in the reaction. It is a radical reaction. Irradiation will cleave the $\ce{Cl-Cl}$ bond and yield chlorine radicals ($\ce{Cl*})$. These will abstract hydrogen atoms …
11
votes
Accepted
What criteria have to be met to term a carboxylic acid a 'fatty acid'?
I suggest to consult the IUPAC Compendium of Chemical Terminology, aka the Gold Book for a definition of fatty acids!
In a narrow sense, fatty acids are defined as
aliphatic monocarboxylic acids …
15
votes
reaction of diketone with ammonium carbonate at 100-115 degree celsius
1,4-diketones are likely to give pyrroles in a Paal-Knorr reaction.
9
votes
Accepted
What results from the reaction of 4-phenylbutanoyl chloride in presence of AlCl3?
My guess was that an other molecule of 4-phenylbutanoyl chloride would react with the phenyl [...]
Your guess is not that bad and it seems that you have identified the type of reaction.
What i …
6
votes
Accepted
Oxidation of styrene with permanganate
In the heterogenous permanganate oxidation of styrene, that is when the reaction is performed in dichloromethane with potassium permanganate on a solid support (such as aluminium oxide), the reaction …
2
votes
P-phenylenediamine Production Process
React benzene with chlorine in the presence of $\ce{FeCl3}$ to yield chlorobenzene.
According to Ullmann's Encyclopedia of Industrial Chemistry:
Most monochlorobenzene is now produced from benzene …
1
vote
Accepted
Ozonide v/s Ozonoid
I've seen the term ozonoide now and then, both in German and English texts.
It was used for the the primary, as well as for the secondary ozonide. Interestingly, throughout these texts, you'll find …
0
votes
Reaction of Benzene with 2-methylpropene?
I took the liberty and corrected the title of your question, assuming that the "ethylene with two methyls" is 2-methylpropene (isobutene). Over here, this classic reaction is known as Friedel-Crafts a …
3
votes
Accepted
What route to take in converting ethanol to crotonic acid?
Allylic bromination and subsequent hydrolysis might be replaced by an allylic oxidation of the butene using selenium dioxide - if that's inorganic enough for you ;)
But I'm wondering whether there's …
2
votes
Accepted
What is the pKa of 2-methyl-2,4-pentanediol?
Do you mean 2-methyl-2,4-pentanediol?
The $pK_a$ values of 2-propanol (isopropanol) and 2-methylpropan-2-ol (tert. butanol) are 16.5 and 17, respectively and I'd expect your diol to be in this range …
3
votes
explain the reaction mechanism
HBr reacts with ROH?
Exactly. It's just a nucleophilic substitution.