It would 3 because if you read it tells you the answer
Answer:
1.
Since both components of these solutions have the same molar mass, mole fractions would be the same as mass fractions.
0.110 atm = (2/3)(Pi) + (1/3)(Pn) [1]
0.089 atm = (1/3)(Pi) + (2/3)(Pn) [2]
2*[1] - [2]:
(2)(0.110) - 0.089 atm = Pi
Pi = 0.131 atm
2*[2] - [1]:
(2)(0.089) - 0.110 atm = Pn
Pn = 0.068 atm
2.
The hydroxyl (-OH) group on the end of a longer 1-propanol molecule makes it more polar than IPA. It follows that the intermolecular forces between 1-propanol are stronger than those of IPA and thus the vapor pressure of 1-propanol should be lower than IPA.
Explanation:
Answer:
The molecular formula of a compound represents molecular mass of the substance. For example, the molecular mass of water molecule (H2O) is 18u.
(iv) The molecular formula of any compound gives the name, and actual number of atoms of each kind present in one molecule of the substance. For example, the formula for water is H2O. This means that every molecule of water is made up of 2 atoms of hydrogen and one atom of oxygen.
Answer:
Energy is released when bonds are broken, and energy is absorbed when bonds are formed.
<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.