What is the configuration of 2 methyl 1 butanol?
2-Methyl-1-butanol
| PubChem CID | 8723 |
|---|---|
| Structure | Find Similar Structures |
| Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
| Molecular Formula | C5H12O or CH3CH2CH(CH3)CH2OH |
| Synonyms | 2-METHYL-1-BUTANOL 2-Methylbutan-1-ol 137-32-6 1-Butanol, 2-methyl- Active amyl alcohol More… |
What combination yields 2-Methyl-2-butanol?
2-methyl-2-butanol is an alcohol with the formula C5H11OH. 2-methyl-2-butanol is comprised of butane, an alkyl chain of four carbons. This chain is substituted at R2 with a methyl group CH3– and an alcohol group OH-. It is synthesized by the reaction of 2-methyl-2-butene with water in the presence of an acid catalyst.
What is the molar mass of 2 Methyl 2-butanol?
2-methylpentan-2-ol is a member of the class of compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). 2-methylpentan-2-ol is soluble (in water) and an extremely weak acidic compound (based on its pKa).
What is the common name for 2 Methyl 1 butanol?
(S)-2-Methyl-1-butanol, also known as sec-butylcarbinol or 2-methyl butanol-1, belongs to the class of organic compounds known as primary alcohols.
Is 2 butanol a secondary alcohol?
2-Butanol, or sec-butanol, or sec-butyl alcohol, or s-butyl alcohol, is a four-carbon chain, with the OH group on the second carbon. (Since the alcoholic carbon is connected to two other carbons, it is secondary, hence the prefix “sec”.) It is used as a solvent and an intermediate in the manufacture of other compounds.
Is 2 Methyl 1-butanol a tertiary alcohol?
Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). 2-Methyl-2-butanol is a pungent tasting compound.
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Structure for FDB011925 (2-Methyl-2-butanol)
| Synonym | Source |
|---|---|
| 2-Methyl-2-butanol | ChEBI |
| 2-Methyl-2-butanol (tert-amyl alcohol) | HMDB |
What is the boiling point of 2 Methyl 2 butanol?
Production. Since the 1950s, most 1-butanol is produced by the hydroformylation of propene (oxo process) to preferentially form the butyraldehyde n-butanal. Typical catalysts are based on cobalt and rhodium. Butyraldehyde is then hydrogenated to produce butanol.
What is the melting point of 2-methyl-2-butanol?
Specifications
| Density | 0.805 g/mL |
|---|---|
| Melting Point | -12°C |
| Boiling Point | 101°C to 103°C |
| Flash Point | 20°C (68°F) |
| Assay Percent Range | 0.98 |
What is the common name of 2 Methylpropan 2 OL?
| IUPAC Name | 2-methylpropan-2-ol |
|---|---|
| Alternative Names | tert-Butanol tert-Butyl alcohol 2-Methyl-2-propanol 2-Methylpropan-2-ol Trimethylcarbinol t-Butanol |
| Molecular Formula | C4H10O |
| Molar Mass | 74.123 g/mol |
| InChI | InChI=1S/C4H10O/c1-4(2,3)5/h5H,1-3H3 |
What were the two products of reacting 2-methyl-2-butanol with sulfuric acid?
The dehydration of 2-methyl-2-butanol was performed using sulfuric acid and phosphoric acid in order to synthesize alkene products 2-methyl-1-butene and 2-methyl-2-butene.