Reactivity is the name your looking for I believe.
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:
See attached picture.
Explanation:
Hello!
In this case, since C2H3Cl is an organic compound we need a central C-C parent chain to which the three hydrogen atoms and one chlorine atom provides the electrons to get all the octets except for H as given on the statement.
In such a way, on the attached picture you can find the required Lewis dot structure without formal charges and with all the unshared electron pairs, considering there is a double bond binding the central carbon atoms in order to compete their octets.
Best regards!
The answer to this question is 2 and 3
Answer and Explanation:
Two hydrogen atoms, each containing one electron, approach each other in the formation of a molecule of hydrogen. Each atom needs a total of two electrons to fill their outermost energy level and make them stable. The best choice is to share their single electrons. Hence, a pair of bonding electrons is shared between the hydrogen atoms in the molecules.
This constitutes a single covalent bond. Hence, the correct option is B)