Oxyanions | Sulfur ions

Thiocarbonate

Thiocarbonate describes a family of anions with the general chemical formula CS3−xO2−x (x = 0, 1, or 2): * for x = 2 it is monothiocarbonate ion CO2S2− * for x = 1 it is dithiocarbonate ion COS2−2 * for x = 0 it is trithiocarbonate ion CS2−3 Like the carbonate dianion, the thiocarbonate ions are trigonal planar, with carbon atom at the center of triangle, and oxygen and sulfur atoms at the peaks of the triangle. The average bond order between C and S or O is 4/3. The state of protonation is usually not specified. These anions are good nucleophiles and good ligands. Thiocarbonates are salts of those ions as well (e.g. sodium dithiocarbonate Na2COS2). Thiocarbonates are esters of thiose ions as well. They contain trigonal planar divalent functional groups similar to these anions. (Wikipedia).

Thiocarbonate
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Making Snakes From a Chemical

In this video we are going to make mercury thiocyanate which is an interesting, highly toxic mercury salt when burned. Patreon: https://www.patreon.com/thyzoid Discord: https://discord.gg/UrjAt44HWH (Let me know if the discord link does not work) Instagram: https://www.instagram.com/thyzo

From playlist Organic Chemistry

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Total Synthesis of Bipolamine I

An organic chemistry minilecture on the Total Synthesis of Bipolamine I by Xiang Qiu and Joshua G. Pierce*. It features a highly effective hydrogen auto-transfer aminoallylation, an unusual manganese promoted oxidative cyclization and a radical reduction/acetalization sequence. SUPPORT T

From playlist Total Synthesis

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Synthesis Workshop: Talatisamine Total Synthesis (Episode 22)

In this Total Synthesis episode, we check out the Inoue group's approach to talatisamine. Parent reference: Angew. Chem. Int. Ed. 2020, 59, 479-486. Other references (in order of appearance: For structural work, see: (a) Tetrahedron 1971, 27, 819-822. (b) Acta Crystallogr. Sect. E 2011,

From playlist Total Synthesis

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Making a Compound With a Great Smell: Benzoin

In todays video we are going to make some benzoin. Benzoin is an organic chemical with a great smell. It is made via the benzoin condensation of benzaldehyde (which is actually an addition reaction). As a catalyst I am using highly toxic potassium cyanide which is why you should not repeat

From playlist Organic Chemistry

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Making Calcium Peroxide (CaO2)

In today’s video we are making calcium peroxide from sodium hydroxide, calcium chloride and hydrogen peroxide. Calcium peroxide is an oxidizing agent and it could be used to make oxygen by simply heating it. Our yield was low but we managed to make some. Just to put it somewhere: the produ

From playlist Inorganic Chemistry

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Ethyl Chloroacetate a Deadly Precursor to Many Pharmaceuticals

In this video ethyl chloroacetate which is a precursor to many pharmaceuticals will be prepared. We will make it by doing an esterification reaction involving chloroacetic acid, ethanol, sulfuric acid and a lot of patience. Ethyl chloroacetate is a toxic liquid used to make chloroacetamide

From playlist Organic Chemistry

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Thiophosgene. Sulfur analogue of phosgene

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From playlist Unique chemicals!

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Making Chromyl Chloride

In this video we are making chromyl chloride which is a potent volatile carcinogen. Chromyl chloride (CrO2Cl2) is this red fuming liquid. It can be used to oxidize toluene to benzaldehyde and to oxidize a lot of other reagents. On my instagram and reddit theres plenty of other pictures of

From playlist Inorganic Chemistry

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NITRATION TIME! Making A Chemical Called Nitrobromobenzene

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From playlist Organic Chemistry

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Synthesizing Sulfur Dichloride: A Noxious Liquid That You DON'T WANT | Thionyl Chloride (Part 1)

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From playlist Chemical madness

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2021 Heterocyclic Chemistry Lecture 5

Lecture 5 - Furans and thiophenes

From playlist Heterocyclic Chemistry 2021

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Making Silicone Oil - An Oil With Everyday Uses #99

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From playlist Organic Chemistry

Related pages

Symmetry group | Trigonal planar molecular geometry | Carbonate