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!
Answer:
Fe + 3CuNO₃ → Fe(NO₃)₃ + 3Cu
Explanation:
- Copper (I) nitrate = CuNO₃ (Nitrate, NO₃⁻, always has a charge of -1).
- Iron (III) nitrate = Fe(NO₃)₃ (That way the compound has an overall neutral charge)
Writing the equation using symbols leaves us with:
- Fe + CuNO₃ → Fe(NO₃)₃ + Cu
<em>It is not balanced yet</em>. Now we <u>balance the NO₃ species on the left side</u>:
- Fe + 3CuNO₃ → Fe(NO₃)₃ + Cu
Finally we<u> balance the Cu species on the right side</u>:
- Fe + 3CuNO₃ → Fe(NO₃)₃ + 3Cu
A !.!.!.!.!.!!..!.!.!.!.!.!.!.!!.!..!!.!.!.!.!.!.!.!.!.!.!!.!.!.!.!
There are eight bonded electrons in this molecule! :)
hope it helps ..............