Which of the following shows the correct order of the levels of classification form Largest to smallest
1 answer:
You might be interested in
The decomposition reaction for hydrogen peroxide is given below:
2
→ 2
O +
This is a decomposition reaction.
Reactions in which a reactant breaks into two or more products are known as Decomposition reactions.
AB → A + B
here, AB represents the reactant that begins the reaction, and A and B represent the products of the reaction
The decomposition reaction of decomposing hydrogen peroxide is exothermic. When the hydrogen peroxide undergoes a decomposition reaction, heat is also released along with water and oxygen.
Hence the reaction for decomposing hydrogen peroxide is :
2
→ 2
O +
If you need to learn more about Decomposition reaction, click here
brainly.com/question/16987748?
#SPJ4
<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 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.