<span>When cyclohexanol is dehydrated using various means it creates a new hydrocarbon. This new hydrocarbon is called cyclohexene. Cyclohexene is a liquid which has no color, yet has a very strong smell to it. It is used in common industrial processes, but is also considered somewhat unstable due to it's tendency to form peroxides when exposed to light.</span>
K gives 1 electron, and Br takes 1 electron.
<u>Answer: </u>The correct statement is X is the effective nuclear charge, and it increases across a period.
<u>Explanation:</u>
We are given that:
X = number of protons − number of core electrons
Effective nuclear charge is defined as the actual nuclear charge (Z = number of protons) minus the screening effect caused by the electrons present between nucleus and valence electrons. These electrons are the core electrons.
The formula used for the calculation of effective nuclear charge given by Slater is:
where,
= effective nuclear charge
Z = atomic number or actual nuclear charge or number of protons
= Screening constant
The effective nuclear charge increases as we go from left to right in a period because nuclear charge increases with no effective increase in screening constant.
Hence, the correct answer is X is the effective nuclear charge, and it increases across a period.
Many electrophilic aromatic halogenations require the presence of an aluminum trihalide as a catalyst. We generally acetylated the amino group as protection. Now, this acetanilide can be brominated at Ortho or para position. An atom that is attached to an aromatic system usually hydrogen is replaced by an electrophile is an organic reaction which is called Electrophilic aromatic substitution. There are what you called important electrophilic aromatic substitutions they are aromatic nitration, aromatic sulfonation, aromatic halogenation and acylation and alkylating Friedel-Crafts reaction. Aromatic bromination is an electrophilic aromatic substitution (EAS) reaction, which will require benzene to act as a nucleophile to acquire an electrophile. Therefore, any directing groups that activate the ring will make it react more quickly with respect to aromatic bromination. Acetanilide is a moderately-activated ring <span>having a decent EWG.</span>
