Answer: Christine Herman & L.G Wade Jr., "2010". Organic Chemistry: Reaction of Alkane, 7e, Pearson Education, Radford University, Radford, VA.
Explanation:
This is an edited book. The Harvard reference style was used in the following order:
Authors name
Year of publication
Title
Edition
Publisher
Place of publication.
Note that the title of book should be italicized with capitalization of first word.
Answer: Uhm you answered your own question...
Explanation:
The majority of the mass of the atom is located in the nucleus. Remember that the nucleus contains both protons and neutrons and therefore, most of the mass of the atom.
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:
the second one seems right :)
Explanation: