The oxidation number of Manganese and the number of d electrons present in each of the given complex has to be given. Concept Introduction: Spectrochemical series: The list of ligands arranged in an ascending order of (Δ) (the splitting of d-orbitals in presence of various ligands). → I - < Br - < SCN - < Cl - < S 2- < F - < OH - < O 2- < H 2 O < NCS - < edta 4- < NH 3 < en < NO 2- < CN - < CO weak-field increasing(Δ) strong-field ligands ligands Crystal field splitting: The energy gap between the splitting of d-orbitals of the metal ion in presence of ligands is known as the crystal field splitting (Δ) . The magnitude of (Δ) is depends on the nature of metal ions and the ligands.
The oxidation number of Manganese and the number of d electrons present in each of the given complex has to be given. Concept Introduction: Spectrochemical series: The list of ligands arranged in an ascending order of (Δ) (the splitting of d-orbitals in presence of various ligands). → I - < Br - < SCN - < Cl - < S 2- < F - < OH - < O 2- < H 2 O < NCS - < edta 4- < NH 3 < en < NO 2- < CN - < CO weak-field increasing(Δ) strong-field ligands ligands Crystal field splitting: The energy gap between the splitting of d-orbitals of the metal ion in presence of ligands is known as the crystal field splitting (Δ) . The magnitude of (Δ) is depends on the nature of metal ions and the ligands.
Solution Summary: The author explains the oxidation number of Manganese and the number d electrons present in each of the given complexes.
Crystal field splitting: The energy gap between the splitting of d-orbitals of the metal ion in presence of ligands is known as the crystal field splitting (Δ). The magnitude of (Δ) is depends on the nature of metal ions and the ligands.
Using the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.
Synthesis of Dibenzalacetone
[References]
Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below.
Question 1
1 pt
Question 2
1 pt
Question 3
1 pt
H
Question 4
1 pt
Question 5
1 pt
Question 6
1 pt
Question 7
1pt
Question 8
1 pt
Progress:
7/8 items
Que Feb 24 at
You do not have to consider stereochemistry.
. Draw the enolate ion in its carbanion form.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
⚫ Separate multiple reactants using the + sign from the drop-down menu.
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4
Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)
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