Answer:
N,N-dimethylacetamide is formed.
Explanation:
- It is an example of a nucleophilic addition-elimination reaction. Here dimethylamine acts as a nucleophile.
- In the first step, dimethyl amine gives nucleophilic addition reaction at carbonyl center of acetyl chloride.
- In the second step, removal of Cl atoms occurs.
- In the third step, deprotonation takes place from amino group to produce N,N-dimethylacetamide.
- Full reaction mechanism has been shown below.
so basically
some fuels have an impurity in them which is sulfur.
When the fuel undergoes combustion, the sulfur reacts with oxygen in the air to form sulfur dioxide.
the sulfur dioxide reacts with water vapour in the air to form sulfurous acid, which is a type of acid rain.
Also
the high pressures inside a car engine may cause nitrogen and oxygen in the air to react and form oxides of nitrogen. the most common compounds formed inside car engines are NO (nitrogen oxide) and NO2 (nitrogen dioxide)
We know, It's atomic formula = C4H10
Now, we know molar mass of C = 12 & H=1
so, it would be: 12*4+1*10 = 48+10 = 58
We have to draw the structural formula of trans-1-bromo-3-isopropylcyclobutane.
The structure is shown below in Figure1.
The molecule trans-1-bromo-3-isopropylcyclobutane has four atoms in the skeleton and Br atom is attached at 1 position and isopropyl group at 3-position.
Trans structure means both groups are in opposite directions.
The answer is D. The teacher describes the plant by saying it has leaves, stems, roots, and fruit. stems are vascular tissue so it can't be C, B, or A.