Here you are looking on the Free Body diagram of a net force of 0N in both the x and y-directions. the only ones that has that condition met is A and C.
<h2>Step 1 : Identify the given </h2>
Volume = 250mL
Density = 1.19 g/ML
<h2>Step 2 . Calculate the mass of HCL </h2>
Density = mass/volume
∴Mass = Density * Volume
= 1.19g/mL* 250mL
= 297,5g
<h2>Step 3 : Calculate the total mass of the solution, given that concentration HCL is 38% </h2>
Mass of the total solution can be calculated by the following :
38% = Mc /297.5 * 100
Mc = 38/100 *297.5
= 113.05grams
• Finally, this means that mass of the total solution of 0.125M HCL i,s 113grams, ,you would use this mass to prepare 250 mL of 0.125 M HCl from concentrated HCl (aq) that is 38.0%
The rate of growth is faster in the (10 - 14) age group and slows down after the age of 14. After the age of 16 the growth is the slowest
Answer : The incorrect option is, The most of the mass of the atom comes from the electron cloud.
Explanation :
There are three basic particles of an atom which are neutrons, protons and electrons.
The nucleus which is present in the center of an atom that contains the neutrons and the protons. The protons are positively charged and neutrons has no charge.
The outer region of an atom contains the electrons and the electrons are negatively charged.
As per given options, the statement which is the most of the mass of the atom comes from the electron cloud is incorrect statement because the most of the mass comes from the nucleus in which protons and neutrons are present.
<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.
