-1.24 v
The reduction of 4-tert-butylcyclohexanone with sodium borohydride would predominantly form the 4-tert-butylcyclohexan-1-ol isomer. This is due to the bulky tert-butyl group favoring the axial position in the chair conformation of the cyclohexane ring, leading to the 1-substituted alcohol as the major product.
A pair of half-reactions with reduction potentials that differ in sign will result in a negative total reduction potential. For example, a half-reaction with a reduction potential of +0.8 V paired with a half-reaction with a reduction potential of -0.7 V would give a negative total reduction potential (+0.8 V - (-0.7 V) = +1.5 V).
the Nernst potential of Sodium is +60mV. most action potentials do not reach +60mV at peak depoloarization. http://openwetware.org/images/thumb/a/a6/Action-potential.jpg/300px-Action-potential.jpg.png
Yes it is. Calcium atom loses electrons more readily in cell reactions than in reactions with air, water and dilute acids.
If you decrease the extracellular sodium concentration, the equilibrium potential of sodium shifts towards a more negative value. This is because there is less sodium available to drive the sodium ions into the cell, causing the equilibrium potential to become more negative.
One mole of benzophenone requires one mole of sodium borohydride for reduction to diphenylmethanol.
In organic chemistry reactions, the reduction of ketones with sodium borohydride is typically carried out by adding the ketone to a solution of sodium borohydride in a suitable solvent, such as ethanol or methanol. The reaction is usually performed at room temperature or slightly elevated temperatures, and the resulting product is often isolated by simple workup procedures like filtration or evaporation.
Yes, sodium borohydride is the same as sodium borohydride. It is a commonly used reducing agent in organic chemistry.
Yes, sodium borohydride is a reducing agent.
Yes, sodium borohydride can reduce ketones.
Yes, sodium borohydride can reduce esters to alcohols.
No, sodium borohydride does not reduce carboxylic acids.
Yes, sodium borohydride can reduce esters to alcohols.
The pKa value of sodium borohydride is approximately 13.
Basic because when sodium borohydride is placed in water, the sodium ion and the borohydride ion split, borohydride abstracts a proton (in the form of H+) from a water molecule.
No, sodium borohydride cannot reduce carboxylic acids.
When phenol is treated with sodium borohydride, a reduction reaction occurs and the oxygen atom in the hydroxyl group of phenol gets reduced to a hydroxide ion. This reaction usually leads to the formation of cyclohexanol as the main product.