Write a reaction mechanism for cinnamaldehyde and acetone
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
The mixture of Polystyrene and Acetone results in the creation of a sticky residue as the Polystyrene beads dissolve into the Acetone. You can use Nail polish remover with Acetone. However, the chemical reaction occurs at a much more rapid pace with pure Acetone.
by grignard reaction.....
yes, some plastics will bond with the use of acetone, the chemical reaction causes the plastic components bond
Acetone can act as a base or and acid, depending on the nature of the other reagents and the reaction conditions.
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
A reaction with alkyl halides in NaI with acetone is by the Sn2 mechanism. The rate for an Sn2 mechanism is directly proportional to the concentration of the nucleophile: rate = k[nucleophile][alkylhalide] If the iodine solution (the nucleophile) is half as concentrated, then the rate will also be halved. rate = k [nucleophile]/2 [alkyl halide]
acetone does not react with potassium dichromate
The mixture of Polystyrene and Acetone results in the creation of a sticky residue as the Polystyrene beads dissolve into the Acetone. You can use Nail polish remover with Acetone. However, the chemical reaction occurs at a much more rapid pace with pure Acetone.
potato
it is an acid catalised reaction, commonly HCl.
by grignard reaction.....
As most catalysts are quite specific in the (or at least the type of) reaction, in others not working at all, I can't give an answer for 'your acetone-reaction'. But to my best knowledge there are very few reactions I can think of being catalysed by acetone; never heard of, you know.
Acetone can act as a base or and acid, depending on the nature of the other reagents and the reaction conditions.
yes, some plastics will bond with the use of acetone, the chemical reaction causes the plastic components bond
Acetone has a carbonyl which is what grignard reacts with; ether however has no such thing (no carbonyl) so it can react easily.
Per Ahlberg has written: 'The mechanism of the condensation of indene with acetone and side reactions' -- subject(s): Acetone, Condensation products (Chemistry), Indenes, Rearrangements (Chemistry)