Both of you are overlooking a pretty big component of the question...the Group I cation isn't being dissociated into water. We're testing the solubility of the cation when mixed with HCl. And this IS a legitimate question, seeing as our lab manual is the one asking.
<span>By the way, the answer you're looking for is "Because Group I cations have insoluble chlorides". </span>
<span>"In order...to distinguish cation Group I, one adds HCl to a sample. If a Group I cation is present in the sample, a precipitate will form." </span>
Answer:
Explanation has been given below
Explanation:
- Attachment of -Cl group at ortho position to acetamido group can be explained in terms of hydrogen bonding formation.
- A hydrogen bonding can be formed between proton attached with N atom in acetamido group and Cl atom at ortho position. This leads to a formation of a stable 5-membered ring structure.
- Hence ortho substitution by Cl is favorable process.
- There is no hydrogen bonding possible between Br and Cl atom in ortho position. Therefore Cl prefers para position to avoid steric hindrance.
- Structure of hydrogen bonded structure has been shown below.
Answer:
bipetal
Explanation:
this is because 2 electrons will be donated by each element, as seen in NO2