The enol carbon or ∝-carbon nucleophile attacks at molecular bromine in the acid-catalyzed α-bromination of a ketone
Treatment of ketones with bromine in the presence of acid will results in formation of a new C-Br bond at the alpha position. The purpose of the acid is to catalysed formation of the enol from ketone , which is active nucleophile in the reaction. This reaction is called haloform reaction which is used to identify the methyl substituted ketone in the presence of aldehyde.
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Answer:
Limited
Explanation:
Once it is used once, it is not reusable. Also, there's a possibility to use ALL the coal there is. That's why it's an unrenewable source, unlike the sun, wind, or water that never ends. Those are renewable
an electrically charged atom or group of atoms formed by the loss or gain of one or more electrons, as a cation (positive ion) , which is created by electron loss and is attracted to the cathode in electrolysis, or as an anion (negative ion) , which is created by an electron gain and is attracted to the anode.
Answer:
Electrons in the outermost energy level of an atom are called VALENCE ELECTRONS.
When we have PH = 9.75
So we can get POH = 14 - 9.75 = 4.25
and when POH = - ㏒[OH-]
by substitution:
4.25 = -㏒[OH-]
∴[OH] = 5.6x10^-5
from this reaction equation:
BOH ↔ B+ + OH-
∴[OH-] = [B+]= 5.6x10^-5 M
and Equ [BOH] = 0.5 m - X
= 0.5 - (5.6x10^-5)
= 0.4999
∴ Kb = [OH-][B+]/[BOH]
= (5.6x10^-5)^2 / 0.4999
= 6.27x10^-9
