True for both academic and industrial environments.<span />
Answer:
The product would have more acidity than Diethyl malonate
Explanation:
For this question, first, we have to start with the structure of the bromination reaction. <u>The bromination would add a "Br" atom</u> in the middle carbon between the ester groups. Therefore, the molecule produced would be <u>diethyl 2-bromomalonate</u> and the formula of this compound fits with the reported by the question:
Now, if we have to analyze the acidity we have to check the <u>most acidic hydrogen</u>. In this case, is the "H" in the middle carbon (red hydrogen). In the Diethyl malonate, we have an <u>inductive effect</u> caused by the carbonyl groups on each side of the middle carbon. In the diethyl 2-bromomalonate, we have this same inductive effect plus the Br atom bonded to the same carbon. Therefore, would be <u>easier to remove the hydrogen</u>. So, diethyl 2-bromomalonate would ba more acidity than Diethyl malonate.
See figure 1
I hope it helps!
Answer:
New Moon
Explanation:
Spring tides occur during new moons when the Sun and the moon are aligned, Pulling together creating big tides.
C because a series circuit only has one loop so it’s C
Answer:
Tellurium
Explanation:
Technetium's position on the periodic table is 43 and Tellurium's is 52