Naming Coordination Compounds - Chemistry
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- Опубликовано: 14 янв 2018
- This chemistry video tutorial provides a basic introduction into naming coordination compounds. It contains plenty of examples and practice problems on the nomenclature of coordination compounds. It discusses how to determine the oxidation state of the transition metal cation and how to name it when the complex ion is cation and when it's the anion.
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For anyone confused on why we use latin endings for some of these...If the ligand part is a CATION we use regular names like Cobalt. However if its an ANION we use the latin name...Colbaltate.
Not the Latin name we add an ate to the Latin name eg : argentium argentate
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It’s really a wonderful video to learn nomenclature of co-ordination compounds
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Small thing I noticed in the video as that you're using older naming conventions. The current IUPAC-recommendation is to call Cl- ligands "chlorido" instead of "chloro", Cn- ligands "cyanido" instead of "cyano", and the same with other ligands ending in "-ide" or "-te". Lots of older sources will still use the old nomenclature but this is technically incorrect.
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number of ligands, then ligand name (place ligands in alphabeitcal order), transition metal, transition metal's oxidation state as the number, then anion
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sir thank you for the video! i came to discover something that when there is anion complex the metal ion name would be written as cobaltate ( ate ) but when its cation complex, the metal ion would be written as the original name of the element. like cobalt. ^_^
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Hi, I would just like to ask if we could also use chlorido instead of chloro?
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Nice Video that prvides mostly correct information. However, a complex (coordination compound) has to be wrtitten in square brackets, you're often forgetting that. And BTW, I never heard of hexachloroplatinate(II), but hexachloroplatinate(IV)
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for iupac standards aren't ligand anions like chloro written as chlorido and aren't the latin names disregarded so you would still put down Iron(III) rather than ferrate
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Sir in the second compound shouldn't the chloride part be chlorido instead of chloro since the system has changed?
So shouldn't the compound be
pentaammine chlorido cobalt (III) chloride?
Just a question, how did you get the charge on CN to be -1?
Sr. When halides eg chlorine comes inside the coordination entity is it named as chlrido?
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In the second example, why is the chlorine inside the cation complex not considered for calculating oxidation state of the central metal atom?
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