Answer:
See figure 1
Explanation:
On this case we have a <u>base</u> (methylamine) and an <u>acid</u> (2-methyl propanoic acid). When we have an acid and a base an <u>acid-base reaction </u>will take place, on this specific case we will produce an <u>ammonium carboxylate salt.</u>
Now the question is: <u>¿These compounds can react by a nucleophile acyl substitution reaction?</u> in other words <u>¿These compounds can produce an amide? </u>
Due to the nature of the compounds (base and acid), <u>the nucleophile</u> (methylamine) <u>doesn't have the ability to attack the carbon</u> of the carbonyl group due to his basicity. The methylamine will react with the acid-<u>producing a positive charge</u> on the nitrogen and with this charge, the methylamine <u>loses all his nucleophilicity.</u>
I hope it helps!
Hi!
The Samurai is what I would attribute to the memory of Ancient<span> Japan.</span>
Answer:
Mechanical advantage is a measure of the force amplification achieved by using a tool, mechanical device or machine system. The device preserves the input power and simply trades off input forces against movement to obtain a desired amplification in the output force. The model for this is the law of the lever.
Explanation:
Answer:
Yes it is hard. For some of us. I already gave up, but now hes coming back. Id say sometimes its useless to get his attention if he never even pays attention to you anyways. It sucks because its so hard to get then to notice you for once.
Explanation:
Answer:
RbF
mgo
nh4cl
because electrons are lost by and element forming a cation and gained by the other element forming an anion and held together by electrostatic forces