The answer will be 17.9 grams
Answer:
0.00000045 m is the wavelength of blue light in decimal
I believe that the answer is B
<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:
There will be 3 peaks.
Relative height of the atomic peaks would be; 158, 160 and 162
Explanation:
We are told that Bromine has two isotopes namely 79Br and 81Br in a 1 : 1 ratio (50 : 50).
This means that a compound which contains 1 bromine atom will have two peaks in the molecular ion region but it depends on which bromine isotope is contained in the molecular ion.
Thus;
Relative height of atomic peaks is given by;
m/z = 79Br¯ 79Br+ = 158
79Br¯ 81Br+ = 160
81Br¯ 81Br+ = 162