Answer:
Carbon is also found in the atmosphere where it's a part of carbon dioxide gas emitted when fossil fuels are burned and when living organisms breathe. It's in organic matter in the soil, and it's in rocks. But far and away the most carbon on Earth is stored in a surprising place: the ocean. Carbon is also found in the atmosphere where it's a part of carbon dioxide gas emitted when fossil fuels are burned and when living organisms breathe. It's in organic matter in the soil, and it's in rocks. But far and away the most carbon on Earth is stored in a surprising place: the ocean.
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Answer:
0.004522 moles of hydrogen peroxide molecules are present.
Explanation:
Mass by mass percentage of hydrogen peroxide solution = w/w% = 3%
Mass of the solution , m= 5.125 g
Mass of the hydrogen peroxide = x



Mass of hydregn pervade in the solution = 0.15375 g
Moles of hydregn pervade in the solution :

0.004522 moles of hydrogen peroxide molecules are present.
The grey liquid is related to the white liquids because the change in colour is the result of a chemical change/reaction between the two white liquids.
Answer:
There are 1.8×1024 atoms in 1.5 mol HCl
Explanation:
<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.