personally I like all of them. shuch masterpiece.
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ok but can you synthesize an amine?
here's how:
-start with a carboxylic acid, such as acetic acid better known as vinegar
-throw SOCl2 at it, better known as thionyl chloride. it stinks, yes, but you want an amine. This step gives you the acyl chloride intermediate. It's a common mistake to think you can just go from a carboxylic acid to an amine, but you can't since they're not reactive enough. That's why we made an acyl chloride intermediate.
-throw TWO EQUIVALENTS of ammonia, NH4, or whatever amino derivative you want to form at the acid chloride and voila there is you amine you weeb.
here's how:
-start with a carboxylic acid, such as acetic acid better known as vinegar
-throw SOCl2 at it, better known as thionyl chloride. it stinks, yes, but you want an amine. This step gives you the acyl chloride intermediate. It's a common mistake to think you can just go from a carboxylic acid to an amine, but you can't since they're not reactive enough. That's why we made an acyl chloride intermediate.
-throw TWO EQUIVALENTS of ammonia, NH4, or whatever amino derivative you want to form at the acid chloride and voila there is you amine you weeb.
nooo! Diels and Alder are the names of the scientists who discovered the reaction
basically you take a diene (a carbon molecule with 2 double bonds) and a dienophile (something that reacts with a diene, usually a single alkene) and have them react with heat
the result is TWO new carbon-carbon bonds, forming a cyclohexENE! (that's a cyclohexane with 1 double bond)
it's pretty convenient if you ever need a cyclohexene :3c
basically you take a diene (a carbon molecule with 2 double bonds) and a dienophile (something that reacts with a diene, usually a single alkene) and have them react with heat
the result is TWO new carbon-carbon bonds, forming a cyclohexENE! (that's a cyclohexane with 1 double bond)
it's pretty convenient if you ever need a cyclohexene :3c
Maybe I'll re-learn about it again. Last time was more than 4 years ago.Jonarwhal wrote: 2rn49
I'm in organic now and omg omg have your heard about the diels alder reaction? It's so cool!GPR wrote: 3z6d6o
It's been a long time since last time I learned about chemistry, especially organic chemistry.
Benzene is probably more useful than cyclohexene.Jonarwhal wrote: 2rn49
nooo! Diels and Alder are the names of the scientists who discovered the reaction
basically you take a diene (a carbon molecule with 2 double bonds) and a dienophile (something that reacts with a diene, usually a single alkene) and have them react with heat
the result is TWO new carbon-carbon bonds, forming a cyclohexENE! (that's a cyclohexane with 1 double bond)
it's pretty convenient if you ever need a cyclohexene :3c
good drink I sayYyottaCat wrote: d3g2y
Benzene is probably more useful than cyclohexene.Jonarwhal wrote: 2rn49
nooo! Diels and Alder are the names of the scientists who discovered the reaction
basically you take a diene (a carbon molecule with 2 double bonds) and a dienophile (something that reacts with a diene, usually a single alkene) and have them react with heat
the result is TWO new carbon-carbon bonds, forming a cyclohexENE! (that's a cyclohexane with 1 double bond)
it's pretty convenient if you ever need a cyclohexene :3c