Answer:
Here's what I get
Explanation:
(a) Intermediates
The three structures below represent one contributor to the resonance-stabilized intermediate, in which the lone pair electrons on the heteroatom are participating (the + charge on the heteroatoms do not show up very well).
(b) Relative Stabilities
The relative stabilities decrease in the order shown.
N is more basic than O, so NH₂ is the best electron donating group (EDG) and will best stabilize the positive charge in the ring. However, the lone pair electrons on the N in acetanilide are also involved in resonance with the carbonyl group, so they are not as available for stabilization of the ring.
(c) Relative reactivities
The relative reactivities would be
C₆H₅-NH₂ > C₆H₅-OCH₃ > C₆H₅-NHCOCH₃
Answer:
addition polymerization
Explanation:
In addition polymerization, the monomers are simply joined to each other to form a polymer having the same empirical formula as the monomer but of higher relative molecular mass. The monomers in addition polymerization are usually simple unsaturated molecules such as alkenes.
We can deduce the reaction to be an addition polymerization because of the the attachment of n to both the unsaturated monomer and the saturated polymer without the loss of any small molecule. If it was a condensation polymerization, there would have been an accompanying loss of a small molecule such as water.
Answer:
How does methane gas affect the environment?
If methane leaks into the air before being used — from a leaky pipe, for instance — it absorbs the sun's heat, warming the atmosphere. For this reason, it's considered a greenhouse gas, like carbon dioxide.
Explanation:
The answer is four hundred
Ca(s)+2Hcl(aq) ------>CaCl2(s)+H2(g)
