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algol13
3 years ago
15

7. How many electrons can a single orbital hold?

Chemistry
2 answers:
Nat2105 [25]3 years ago
8 0
“It can hold two electrons”
levacccp [35]3 years ago
5 0

Answer:

2 electrons

Explanation:

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Why are 1-chlorobutane and 2-chlorobutane structural isomers?.
Nutka1998 [239]

Answer: they both have the same molecular formula but different structural formulae

Explanation:

hope this helps :)

6 0
2 years ago
A can was filled with crushed ice, sealed, and massed. The ice was melted by slowly warming the can and its contents. No water v
Lera25 [3.4K]

Answer:

A) The mass would be the same.

Explanation:

Since there is no loss of any particle to vapor during the phase change process from solid to liquid, the mass of the before and after the process will remain the same.

  • In this way, the law of conservation of mass is obeyed.
  • Mass is the amount of matter contained in a substance.
  • Since there is no room for escape or matter loss, the mass will remain the same.
8 0
3 years ago
Read 2 more answers
Rank these compounds by their expected boiling point? CH4 CH3Cl CH3OH? Lowest to highest; 10+ for the best explanation. Thank yo
docker41 [41]
Methane, CH4, would have the lowest boiling point among the three since it has the lowest number of carbon and has no functional groups. Methanol would have the highest boiling point since it has a functional group which contains hydrogen bonding which much stronger than the one in CH3Cl. Hope this helps.<span />
3 0
3 years ago
Read 2 more answers
Taking advantage of their large differences in pKa values, describe how a mixture of phenol and benzoic acid in diethyl ether so
Marat540 [252]

Answer:

By adding bicarbonate.

Explanation:

The pka of the phenol (C₆H₅OH) is 10 and the pka of the benzoic acid (C₆H₅COOH) is 4, which means that the benzoic acid is a stronger acid than phenol, so if we want to separate phenol from benzoic acid in diethyl ether we need to first use a weak base that will react with benzoic acid and not with the phenol:  

C₆H₅-COOH + HCO₃⁻  ⇄  C₆H₅-COO⁻  +  H₂CO₃

C₆H₅-OH + HCO₃⁻  ⇄  no reaction

The reaction of the benzoic acid with bicarbonate will produce the benzoate ion that will be soluble in the aqueous layer, while the phenol will remain dissolved in the organic layer, so we can separate the two of them by the separation of the two immiscible layers.      

Having the two layers separated, the benzoic acid can be recovered from the aqueous layer by adding HCl:

C₆H₅-COO⁻ + HCl  ⇄  C₆H₅-COOH + Cl⁻

<u>This acid will precipitate from the aqueous solution, and the solid can be isolated by filtration</u>.  

The phenol in the organic layer can be dissolved into an aqueous layer by the adding of a strong base like NaOH:

C₆H₅-OH + OH⁻  ⇄  C₆H₅-O⁻ + H₂O

The phenoxide ion soluble in the aqueous layer can be recovered later by the adding of HCl, which will form the original phenol:

C₆H₅-O⁻ + HCl  ⇄  C₆H₅-OH + Cl⁻  

<u>The precipitated phenol can be isolated by filtration. </u>

This way we can separate a mixture of phenol and benzoic acid in diethyl ether solution.  

I hope it helps you!

6 0
3 years ago
Which of the following contains the most atoms?
aksik [14]

Explanation:

9.0122 g be Maybe, sorry i don't think so

8 0
3 years ago
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