Answer:
a) 2-bromopyrrole
Explanation:
Our options for this questions are:
a) 2-bromopyrrole
b) 2,3-dibromopyrrole
c) N-bromopyrrole
d) 3-bromopyrrole
To understand how the reaction works we have to start with the <u>resonance structures</u>. (Figure 1), on these structures, we will obtain a n<u>egative charge on carbon 2</u> in the pyrrole ring, therefore on this carbon we can generate an attack to an electrophile.
The second step is to check how the mechanism take place. An <u>electrophile is generated</u> by the 
and 
. This electrophile can be <u>attacked</u> by the negative charge on carbon 2 producing the 2-bromopyrrole. (See figure 2).
I hope it helps!
Answer:
A. 32.06 g/mol
Explanation:
The molar mass units are always g/mol
Answer:
A carboxylate salt and water
Explanation:
A carboxylic acid is an organic compound that has general formula RCOOH, where R is a carbon chain. Because it's an acid, the neutralization will happen when it reacts with a base, such as NaOH.
When this reaction occurs, the base will dissociate in Na⁺ and OH⁻, and the acid will ionize in RCOO⁻ and H⁺, so the products will be RCOO⁻Na⁺ (a carboxylate salt) and H₂O (water).
Active sites in enzymes are where substrates bind. Once they bind, a catalytic reaction occurs as a complex between substrate and enzyme is formed. Enzymes are termed as biocatalysts or simply catalysts since they speed up the catalytic reaction. After the reaction, they simply revert back to their original form, after having adjusted to fit with substrate.
