Are nails in a jar with water a chemical change
1 answer:
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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:
Please find the structure attached as an image
Explanation:
Based on the characteristics ending name (-ene) of the organic compound above, it belongs to the ALKENE GROUP. Alkenes are characterized by the possession of a carbon to carbon double bond (C=C) in their structure.
- But-3-ene tells us that the organic compound has four straight carbon atoms with the C=C (double bond) located on the THIRD carbon depending on if we count from right to left or vice versa.
- 2 methyl indicates that the methyl group (-CH3) is located as an attachment on the second carbon (carbon 2).
N.B: In the structure attached below, the counting is from the left to right (→).
