Answer:
The hydrolysis in aqueous HCl of compound A can lead to the formation of a carboxylic acid and an alcohol.
Explanation:
The picture shows the structures of compound A, benzoncaine and the possible products of the proposed reaction.
The acidic hydrolysis is the inverse of the esterification reaction. Therefore, the ester group of compund A will react to form the equivalent carboxylic acid and alcohol.
In order to form benzocaine, the hydrolysis happens in with the nitrile group.
Answer:
See below
Step-by-step explanation:
You won't see much happening. The solution is saturated, so the salt will fall to the bottom of the container and sit there. It will not dissolve.
However, at the atomic level, Na⁺ and Cl⁻ ions are being pulled from the surface of the crystals and going into solution as hydrated ions. At other places, Na⁺ and Cl⁻ ions are returning to the surface of the crystals.
The process is
NaCl(s) ⇌ Na⁺(aq) + Cl⁻(aq)
The rates of the forward and reverse processes are equal, so you see no net change.
The reducing agent will itself be oxidized.
The oxidation number of carbon goes form 0 to +2. Therefore, it is the reducing agent.
Answer: There are three main places where volcanoes originate: Hot spots, Divergent plate boundaries (such as rifts and mid-ocean ridges), and. Convergent plate boundaries (subduction zones)
Explanation:
Volcanoes often form in the areas where tectonic plates make contact. The friction created between two plates by the constant movement melts the Earth's crust, causing the rock underneath the crust to turn into magma due to the great temperatures created by friction. ... Volcanoes may be formed at subduction zones
