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maria [59]
2 years ago
5

16.

Chemistry
1 answer:
il63 [147K]2 years ago
8 0
D is the answer how do you not know this a third grader could get this
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Which of the following BEST describes the process of evolution by natural selection?
svlad2 [7]

Answer:

<em>The correct option is B)  a gradual change of the traits of a species over time</em>

Explanation:

The theory of natural selection explains the gradual changes which occur in the population of a species over time. According to natural selection, those organisms which are better adapted to live in an environment survive and pass on their traits to their offsprings. As a result, the traits of a species tend to change over time through the process of evolution. Evolutionary changes do not occur rapidly, instead, they can take many years to occur.

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The following compound has been found effective in treating pain and inflammation (J. Med Chem. 2007, 4222). Which sequence corr
love history [14]
<h3><u>Full Question:</u></h3>

The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?

A) 1 < 2 < 3

B) 2 < 3 < 1

C) 3 < 1 < 2

D) 1 < 3 < 2

<h3><u>Answer: </u></h3>

The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.

Option B

<h3><u>Explanation. </u></h3>

Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.

A carbonyl compound is a sp^2 hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.

In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.

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