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!
<span>The American Council for an Energy-Efficient Economy works to (c) </span>invest in clean energy technologies that will strengthen the economy.
Their aim is to promote energy efficiency which will ultimately benefit the economy and the environment.
Answer:
Hmm
Explanation:
Elemental antimony adults a layer structure (space group R3m No.166) in which layers consist of fused, ruffled, six-membered rings. The nearest and the next nearest neighbors form and irregular octahedral complex, with the 3 atoms in each layer slightly closer than 3 atoms in the next
Electric configuration : 4d^10 5s^2 5p^3
Answer:
an uneven charge between the oxygen molecule and 2 hydrogen molecules
Explanation:
Answer: alcohols
Explanation:
The carbonyl group refers to C=O. It is contained in aldehyde, Ketones, carboxylic acids , esters, amides and acyl chlorides. They are not found in alcohols. The alchols are generally ROH. They do not contain any carbon-oxygen unsaturated bond in their structure hence the answer.
