The reaction will generally form more reactants than products.
Answer:
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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.
CaI₂ + Hg(NO₃)₂ --------->HgI₂ + Ca(NO3)2
2Al + 3Cl₂ --------->2AlCl3
Ag + HCl ------->AgCl + H2
C2H2 + 5O2 --------> 4CO2 + 2H2O
MgCl₂ --------->Mg + Cl2