Yes, the chair confirmation of cyclohexane is more stable than the boat confirmation. The decreased stability of the of the boat conformation is caused by the nonbonding interactions generated by the close proximity of the 2 hydrogen atoms on c1 and c4 and by the eclipsing of hydrogens along the c2-c3 and c5-c6 bonds.
Boat form of cyclohexane is least stable, half chair form is more table but most sable is complete chair form.
false
Chair form (of hexane) is more stable configuration because out of eight hydrogen four form the equatorial bonds and four axial bonds so its a symmetrical structure and repulsive force among the hydrogens is minimum.
The linear glucose molecule could form a pyranose ring (cyclic formation) by the reaction between the aldehyde group (on C1) and the hydroxyl group (on C5). The configuration could be either a chair form (more stable) or a boat form (less stable), as an alpha-D-glucopyranose or a beta-D-glucopyranose.
Propane, being a GAS but an aliphatic hydrocarbon is soluble in cyclohexane, which is a liquid and a cycloaliphatic hydrocarbon. .
Cyclohexane can form only one mono-substituted alkyl chloride. Because cyclohexane is a symmetrical molecule with only a single type of carbon atom and no stereoisomers will be formed because there are no asymmetric centers, the product will be the same no matter which carbon the chlorine atom attaches to.
they are stable
chair form as the steric repulsions is minimum
All forms/conformations existing in nature of cyclohexane are non-aromatic including boat and chair conformations.Note: Planar or "flat" cyclohexane isanti-aromaticand does not exist in nature due to high instability.
no because unlike cyclohexane which has all single bonds, benzene alterates with double and single bonds. therefore it does not want to freely form the boat and chair conformations
No, each carbon will form a three dimensional tetrahedral bonding.
Chair form (of hexane) is more stable configuration because out of eight hydrogen four form the equatorial bonds and four axial bonds so its a symmetrical structure and repulsive force among the hydrogens is minimum.
Cyclohexane doesn't form ions in water.
The linear glucose molecule could form a pyranose ring (cyclic formation) by the reaction between the aldehyde group (on C1) and the hydroxyl group (on C5). The configuration could be either a chair form (more stable) or a boat form (less stable), as an alpha-D-glucopyranose or a beta-D-glucopyranose.
Propane, being a GAS but an aliphatic hydrocarbon is soluble in cyclohexane, which is a liquid and a cycloaliphatic hydrocarbon. .
Cyclohexane which is a cycloalkanes, has a structural formula of C6H12. It may be written in a condensed form as (CH2)6.
Chair
chair's
Chair can be a noun or a verb: "He wanted to chair the committee" Verb form "She wanted a new chair for the living room" Noun form