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).
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Answer:
I believe it is 3 and 4. I really hope it is but i am positive :)
C.) Newton. & it's S.I. Unit of Force.
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Condenser Lens - This lens system is located immediately under the stage and focuses the light on the specimen.
Covalent example ch4 where carbon is covalently bonded with all 4 hydrogens