Answer:
A. How the concentration of the reactants affects the rate of a reaction
Explanation:
Let's consider a generic reaction.
A + B ⇒ Products
The generic rate law is:
rate = k × [A]ᵃ × [B]ᵇ
where,
- rate: rate of the reaction
- [A] and [B]: molar concentrations of the reactants
As we can see, the rate law shows how the concentration of the reactants affects the rate of a reaction.
Answer:
<u>True</u>
Explanation:
|ndeed, Psychologist Abraham Maslow's sought to describe hierarchy in which the average (or most) humans place their needs. In other words, he believes we as humans have basic needs which we long to satisfy.
On the ranking or hierarchy, according to Maslow the need humans satisfy first is their physiological need. Here's the full hierarchy:
Physiological Needs
↓
Safety Needs
↓
Love/Belonging Needs
↓
Esteem Needs
↓
Self-Actualization
Answer:
0.158 moles
Explanation:
We are given;
9.50 x 10^22 molecules of CO
We are required to determine the number of moles;
We need to know;
1 mole of a compound = 6.022 × 10^23 molecules
Therefore;
9.50 x 10^22 molecules of CO will be equivalent to;
= 9.50 x 10^22 molecules ÷ 6.022 × 10^23 molecules/mole
= 0.158 moles
Therefore, the number of moles are 0.158 moles
I am going to say C. it has to do with the angles
<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.