The solubility of PbBr₂(s) with the presence of 0.500 M of KBr is
2.64 x 10⁻⁵ M.
I don't see the options for an answer, so here is a list of all of the transition metals lol
- <em>Scandium</em>
- <em>Titanium</em>
- <em>Vanadium</em>
- <em>Chromium</em>
- <em>Manganese</em>
- <em>Iron</em>
- <em>Cobalt</em>
- <em>Nickel</em>
- <em>Copper</em>
- <em>Zinc</em>
- <em>Yttrium</em>
- <em>Zirconium</em>
- <em>Niobium</em>
- <em>Molybdenum</em>
- <em>Technetium</em>
- <em>Ruthenium</em>
- <em>Rhodium</em>
- <em>Palladium</em>
- <em>Silver</em>
- <em>Cadmium</em>
- <em>Lanthanum</em>
- <em>Hafnium</em>
- <em>Tantalum</em>
- <em>Tungsten</em>
- <em>Rhenium</em>
- <em>Osmium</em>
- <em>Iridium</em>
- <em>Platinum</em>
- <em>Gold</em>
- <em>Mercury</em>
- <em>Actinium</em>
- <em>Rutherfordium</em>
- <em>Dubnium</em>
- <em>Seaborgium</em>
- <em>Bohrium</em>
- <em>Hassium</em>
- <em>Meitnerium</em>
- <em>Darmstadtium</em>
- <em>Roentgenium</em>
- <em>Copernicium p</em>
Answer:
Axial position
Explanation:
In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equatorial position and the alcohol in the axial position.
The reason for this is that, axial bonds are parallel to each other. If substituents are larger than hydrogen, they experience a greater steric crowding in axial compared to the equatorial position. Therefore, many substituted cyclohexane compounds prefer a conformation in which the larger substituents are in equatorial position.
Answer:
The answer is A
Explanation:
Image A has the same species while image B has more species than A.
Answer:
Al is oxidized while Ag is reduced.
Explanation:
The complete molecular equation is;
3Ag2S + 2Al --> 6Ag + Al2S3
Oxidation half equation;
2Al ------> 2Al^3+ + 6e
Reduction half equation;
6Ag^+ + 6e -------> 6Ag
Overall redox reaction equation;
2Al + 6Ag^+ ----->2Al^3+ + 6Ag
Hence; Al is oxidized while Ag is reduced.
