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Prévost reaction
...mical reaction that involves the stereospecific conversion of alkenes into vicinal dihalides through the reaction with iodine chloride (ICl). This reaction is ...substituted carbon of the iodonium ion, resulting in the formation of the vicinal dihalide.

3 KB (453 words) - 12:52, 21 April 2024
Diol
* '''Vicinal diols''' (or glycols), where the hydroxyl groups are on adjacent carbon ato * '''1,2-diols''' refer specifically to vicinal diols.

3 KB (461 words) - 23:48, 19 April 2024
Geminal
...le. For instance, geminal dihalides are typically more reactive than their vicinal (neighboring carbon atoms) counterparts due to the increased electron-withd * [[Vicinal (chemistry)]]

2 KB (313 words) - 08:35, 19 March 2024
Corey–Winter olefin synthesis
...eactions designed for the preparation of alkenes (olefins) from 1,2-diols (vicinal diols). The process involves the conversion of diols into cyclic sulfates f # Formation of the cyclic sulfate: The vicinal diol is first treated with a sulfuryl chloride (SO2Cl2) in the presence of

2 KB (337 words) - 07:49, 19 March 2024
Diols
* '''Vicinal diols''': The hydroxyl groups are on adjacent carbon atoms. An example is e ...eduction of carbonyl compounds''': Aldehydes and ketones can be reduced to vicinal diols using reducing agents such as sodium borohydride (NaBH_4).

3 KB (365 words) - 15:51, 23 March 2024
Treosulfan
[[Category:Vicinal diols]]

1 KB (147 words) - 03:57, 26 September 2023
Sodium periodate
...odate is widely used in organic synthesis, particularly in the cleavage of vicinal diols to form aldehydes or ketones. This reaction is known as the [[Malapra

2 KB (257 words) - 02:24, 25 March 2024
2,3-Butanediol
...r>'''2,3-Butanediol''' is a [[organic compound]] that is classified as a [[vicinal diol]] (glycol). The compound exists as three [[isomers]], which are 2,3-bu

2 KB (306 words) - 04:57, 6 March 2024
Pinacolone
...important reaction in organic chemistry for the synthesis of ketones from vicinal diols.

2 KB (330 words) - 00:18, 18 April 2024
Alkynyl
...various synthetic routes. One common method is the dehydrohalogenation of vicinal dihalides or the elimination of hydrogen halide from geminal dihalides, usi

2 KB (350 words) - 01:51, 3 April 2024
Bromination
...(Br2) acts as an electrophile and adds to an alkene or alkyne, forming a [[vicinal dibromide]]. This reaction typically requires the presence of a non-polar s

3 KB (341 words) - 18:57, 27 March 2024
Carroll rearrangement
...rticularly useful for synthesizing aldehydes and ketones from 1,2-diols or vicinal diols, which are glycols with two hydroxyl groups on adjacent carbon atoms.

3 KB (371 words) - 08:27, 19 March 2024
Glycol cleavage
...acid (HIO4) in the [[Periodic Acid Schiff (PAS) reaction]], which cleaves vicinal diols (glycols where the hydroxyl groups are on adjacent carbon atoms) to f

3 KB (403 words) - 02:45, 18 April 2024
Periodic acid–Schiff stain
...ntaining a high proportion of carbohydrate material, especially those with vicinal diol groups that can be oxidized to aldehydes.

3 KB (440 words) - 04:52, 22 April 2024
Alkyne
...synthesized through various methods, including the dehydrohalogenation of vicinal or geminal dihalides, and the [[alkyne metathesis]]. Another common method

3 KB (465 words) - 20:07, 19 April 2024
Ethylene glycol
[[Category:Vicinal diols]]

3 KB (434 words) - 22:17, 19 September 2020
Dehalogenation
..., forming a double bond. This process is typical for the dehalogenation of vicinal (neighboring) dihalides and can proceed through E1 or E2 mechanisms, simila

4 KB (514 words) - 20:03, 19 April 2024
Monoctanoin
[[Category:Vicinal diols]]

3 KB (445 words) - 04:11, 27 September 2023
Nystatin Topical
[[Category:Vicinal diols]]

6 KB (884 words) - 14:50, 2 November 2022
Nystatin
[[Category:Vicinal diols]]

7 KB (1,006 words) - 06:51, 16 September 2023