You need to prepare an acetate buffer of pH 5.47 from a 0.809 M acetic acid solution and a 2.20 M KOH solution. If you have 680
1 answer:
You might be interested in
<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.
Answer:
Explanation:
Given that
d= 35 μm ,yield strength = 163 MPa
d= 17 μm ,yield strength = 192 MPa
As we know that relationship between diameter and yield strength
d = diameter
K =Constant
So now by putting the values
d= 35 μm ,yield strength = 163 MPa
------------1
d= 17 μm ,yield strength = 192 MPa
------------2
From equation 1 and 2
K=394.53
By putting the values of K in equation 1
Now when d= 12 μm