Answer:
3-methylthiophene > thiophene > benzene > 2-methylfuran
Explanation:
Primarily, five membered heterocyclic aromatic rings undergo nitration at carbon-2. This is because, nitration at carbon-2 leads to the formation of three resonance structures while attack at carbon-3 yields only two resonance structures, hence it is less stabilized.
The presence of a methyl group which donates electrons promotes the stabilization of the cation formed in the nitration of 3-methylthiophene.
2-methylfuran is the least reactive towards nitration because the 2-position has been blocked by a methyl group.
Answer:
8kJ/mol
Explanation:
since the forward reaction is -8kJ/mol, the backward reaction has the same enthalphy but reversed
Answer:
After measuring the solute, Carl should first dissolve the solid in a small amount of DI water before diluting to the total volume.
Explanation:
To ensure that all the solute dissolves in the solution, first dissolve the solid in less than the total volume of solution needed.
Answer:
748 torr
Explanation:
mmHg and torr are equivalent so, you'll have 748 torr.
2 Ionic bonds form between metal atoms and nonmetal atoms.
4 The less electronegative atoms transfers one or more electrons to the more electronegative atom.
5 The metal atom forms a cation and the nonmetal atom forms an anion.
7 The attraction between ions with an opposite charge forms an ionic bond.