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IRINA_888 [86]
1 year ago
9

Describe the pattern in melting point please!

Chemistry
1 answer:
Degger [83]1 year ago
3 0
It seems to overall decrease.
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Chemistry, please help! Thanks.
Ilya [14]

Answer:

d. The gold(III) ion is most easily reduced.

Explanation:

The standard reduction potentials are

Au³⁺ + 3e⁻ ⟶ Au;   1.50 V

Hg²⁺ + 2e⁻ ⟶ Hg; 0.85 V

Zn²⁺ + 2e⁻ ⟶ Zn; -0.76 V

Na⁺ + e⁻     ⟶ Na; -2.71 V

A <em>more positive voltage</em> means that there is a <em>stronger driving force</em> for the reaction.

Thus, Au³⁺ is the best acceptor of electrons.

Reduction Is Gain of electrons and, Au³⁺ is gaining electrons,  so

Au³⁺ is most easily reduced.

4 0
3 years ago
Does Hornfels have biological origins
anzhelika [568]

Answer:

Hornfels most commonly form in the aureole of granitic intrusions in the upper or middle crust. Hornfels formed from contact metamorphism by volcanic activity very close to the surface can produce unusual and distinctive minerals.

3 0
3 years ago
The melting point of h2o is 0 degrees celsius. this is the same as its:
professor190 [17]
This is the same as its freezing point

hope this helps
6 0
3 years ago
NAME THESE ALCOHOLS. CH3CH2CH2CH2OH AND CH3CH(OH)CH3
ale4655 [162]
"CH3CH2CH2CH2OH " is known by the name of "n-butanol" and "CH3CH(OH)CH3" is known by the name of "<span>Isopropyl alcohol". These two given products are basically alcohols. I hope that this is the answer that you were looking for and the answer has actually come to your desired help. Thanks for joining brainly and getting your questions solved.</span>
3 0
2 years ago
For each of the following pairs of complexes, identify which one you would predict to have the larger Δo value, and explain why.
mash [69]

Answer:

a) [Fe(H2O)6]3+

b) [Fe(CN)6]3−

c) [Ru(CN)6]3-

Explanation:

. [Mn(H2O)6]2+ or [Fe(H2O)6]3+

The both complexes are d5 complexes with the same ligand , water. Water is a weak ligand and note that Mn^2+ often have a crystal field stabilization energy of zero hence

[Fe(H2O)6]3+ will possess a greater ∆o value.

The splitting of d orbitals according to the crystal field theory depends on the;

i)geometry of the complex

ii) nature of the metal ion,

iii)charge on the metal ion,

iv) ligands that surround the metal ion.

When the geometry and the ligands are held constant, the order of crystal field splitting is as follows;

Pt4+ > Ir3+ > Rh3+ > Co3+ > Cr3+ > Fe3+ > Fe2+ > Co2+ > Ni2+ > Mn2+

[Fe(H2O)6]3+ or [Fe(CN)6]3−

[Fe(CN)6]3− will have a greater ∆o because the cyanide ion is a strong field ligand compared to water. A strong field ligand causes a greater splitting of the octahedral crystal field compared to a weak field ligand.

. [Fe(CN)6]3− or [Ru(CN)6]3-

[Ru(CN)6]3- will exhibit a greater crystal field splitting. Crystal field splitting increases with the second and third row transition elements when compared to the crystal field splitting of the first row transition elements. Note that, there is an increase of approximately 30%–50% in Δo on going from a first-row transition metal to a second-row metal and another 30%–50% increase on going from a second-row to a third-row metal when they have the same geometry and oxidation state.

4 0
2 years ago
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