2-Butanol - NIST Chemistry WebBook
Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file. The 3d structure may be viewed using Java or Javascript. Species with the same structure: 2-Butanol. Stereoisomers: 2-Butanol, (R)- (S)-butan-2-ol.
Alcohols - Nomenclature and Properties - Master Organic Chemistry
2014年9月17日 · See how the primary alcohols (1-butanol and 2-methyl-1-propanol) have higher boiling points than the secondary alcohol (2-butanol) which has a higher boiling point than the tertiary alcohol (t-butanol).
Lewis Structure Finder - Wolfram|Alpha
This widget gets the Lewis structure of chemical compounds. Get the free "Lewis Structure Finder" widget for your website, blog, Wordpress, Blogger, or iGoogle.
2-Butanol - Wikipedia
Butan-2-ol, or sec-butanol, is an organic compound with formula C H 3 CH(OH)CH 2 CH 3. Its structural isomers are 1-butanol, isobutanol, and tert-butanol. 2-Butanol is chiral and thus can be obtained as either of two stereoisomers designated as (R)-(−)-butan-2-ol and (S)-(+)-butan-2-ol.
(±)-2-Butanol | C4H10O - ChemSpider
ChemSpider record containing structure, synonyms, properties, vendors and database links for (±)-2-Butanol, 78-92-2.
2-Butanol | C4H10O | CID 6568 - PubChem
2-Butanol | C4H10O | CID 6568 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Structure of 2-Butanol (C4H10O) - Mol-Instincts
The 3D chemical structure image of 2-Butanol is based on the ball-and-stick model which displays both the three-dimensional position of the atoms and the bonds between them.
(S)-butan-2-ol - NIST Chemistry WebBook
Formula: C 4 H 10 O. Molecular weight: 74.1216. IUPAC Standard InChI:InChI=1S/C4H10O/c1-3-4 (2)5/h4-5H,3H2,1-2H3/t4-/m1/s1 Copy. IUPAC Standard InChIKey:BTANRVKWQNVYAZ-SCSAIBSYSA-N Copy. CAS Registry Number: 4221-99-2.
17.2: Properties of Alcohols and Phenols - Chemistry LibreTexts
explain the difference in acidity between two given alcohols or phenols. explain why phenols are more acidic than alcohols. explain, in terms of inductive and resonance effects, why a given substituted phenol is more or less acidic than phenol itself.
3.4. Isomers | Organic Chemistry 1: An open textbook - Lumen …
Chain isomerism. These isomers arise because of the possibility of branching in carbon chains. For example, there are two isomers of butane, C4H10 C 4 H 10. In one of them, the carbon atoms lie in a “straight chain” whereas in the other the chain is branched.