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!
Ethanoic acid ionizes in aqueous solutions to form two ions which are 
and 
<h3>Ionization of ethanoic acid</h3>
Ethanoic acid goes by the chemical formula 
.
In aqueous solutions, it ionizes as a monoprotic acid according to the following equation:
A monoprotic acid is an acid that is able to donate only a proton. Hence, ethanoic acid is said to be monoprotic because it ionizes in aqueous solutions to produce a single
More on ethanoic acid can be found here: brainly.com/question/9991017
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Answer:
a
Explanation:
the others are rude, and rather support this, while a helps to support the ending of white privlige
Um, I think it’s: k is potassium and F is fluorine so potassium Fluoride
