Answer:
It reacts by fizzing and wearing away/dissolving the rock.
Explanation:
Answer:
At equilibrium the rate of the forward reaction is equal to the rate of the backward reaction.
When the product of a reaction at equilibrium is increased the equilibrium will shift left or to the reactant side. As a result the excess product will get converted to reactant. This is in accordance to Le Chatelier's principle.
Le Chatelier's principle states that when a system is subjected to stress the equilibrium will shift in a direction to minimize effect of the stress.
Thus the products added to the system at equilibrium will make the equilibrium shift to the reactant side, the rate of the reverse or backward reaction will increase.
Explanation:
Hope This Helps Amigo!
Answer:
Porque como tu no eres profesional en medicina, no sabes nada sobre las dosis de medicamentos ni de los efectos que pueden tener en tu cuerpo si se administran incorrectamente.
Explanation:
Es logico que solo vayas al medico para que te den la cura allí.
Answer:
The line drawn through points D and E.
Explanation:
Y is a horizontal line and D and E are both on the same line. If a line were drawn it would be within the Y plane.
Answer:
Product A: cis; no
Product B: cis: no
Explanation:
Two common methods of forming oxiranes from alkenes are:
- Reaction with peroxyacids
- Formation of a halohydrin followed by reaction with base
1. Reaction with peroxyacids
(a) Stereochemistry
The reaction with a peroxyacid is a syn addition, so the product has the same stereochemistry as the alkene.
The starting alkene is cis, so the product is <em>cis</em>-2,3-diethyloxirane.
(b) Configuration
The product is optically inactive because it has an internal plane of symmetry.
It will not rotate the plane of polarized light.
2. Halohydrin formation
(a) Stereochemistry
The halogenation of the alkene proceeds via a cyclic halonium ion.
The backside displacement of halide ion by alkoxide is also stereospecific, so a cis alkene gives a cis epoxide.
The product is <em>cis</em>-2,3-diethyloxirane.
(b) Configuration
The cyclic halonium ion has an internal plane of symmetry, as does the product (meso).
The oxirane will not rotate the plane of polarized light.