The answer is B, the heart is the center of the cardiovascular system as one of its main tasks is to distribute blood throughout the body.
We can call a person by the word gentleman and Sir or from his/her real name.
If there is a name/surname you can't make out due to a speaker's manner of speech then I will call him gentleman or Sir or I will ask him his real name. Gentleman is a word that is used for noble person and Sir word is also used in order to give someone respect.
Call a person with his real name is also comes under the manner of speech so we can conclude that we can call a person by the word gentleman and Sir or from his/her real name.
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Principal shell shows the main energy level, in that there are some more energy levels. This is how the atomic structure is defined according to the Quantum Mechanical model of atom. So exactly why do subshells exist and all i don't know
They would find out by studying hard and researching different things on which is more important
<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.