A current is applied to two electrolytic cells in series. In the first, silver is deposited; in the second, a zinc electrode is
1 answer:
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Answer:
The carbocation intermediate reacts with a nucleophile to form the addition product.
Explanation:
The reaction of benzene with an electrophile is an electrophillic substitution reaction. Here the electrophile replaces hydrogen. There is no formation of carbocation as intermediate in the reaction. Infact there is transition state where the electorphile attacks on benzene ring and at the same time the hydrogen gets removed from the benzene. So a transition carbocation is formed.
The general mechanism is shown in the figure.
i) Attack of the electrophile on the benzene (which is the nucleophile)
ii) The carbocation intermediate loses a proton from the carbon bonded to the electrophile.
iii) the carbocation formation is the rate determining step.
iv) There is no formation of addition product.
Thus the wrong statement is
The carbocation intermediate reacts with a nucleophile to form the addition product.
In a a cation-exchange resin, the outlet stream leaving the bed will contain and
.
- A resin or polymer that serves as a medium for ion exchange is known as an ion-exchange resin or cation-exchange resin.
- It is an insoluble matrix (or support structure) made from an organic polymer substrate, typically appearing as tiny (0.25-1.43 mm radius) microbeads that are white or yellowish in color.
- The process is known as cation-exchange resin because the beads are often porous, providing a wide surface area on and inside them where the trapping of ions takes place along with the concomitant release of other ions.
- cation-exchange resin comes in many different varieties. Polystyrene sulfonate is the main ingredient in most commercial resins. Many diverse separation, purification, and decontamination techniques use cation-exchange resin.
- The most typical examples are water filtration and water softening.
To learn more about cation-exchange resin with the given link
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