Oxidized yo aldehyde
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.
You usually reduce a ketone such as propanone using sodium borohydride to propanol.
Yes
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Phenol is an acid while sodium hydroxide a base so it is acid base reaction forming the salt sodium phenoxide and water. C6H5-OH + NaOH = C6H5-ONa + H2O
This doesn't make sense. Google "sodium borohydride msds" to get the MSDS for sodium borohydride.
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.
You usually reduce a ketone such as propanone using sodium borohydride to propanol.
Yes
Erik H. Jensen has written: 'A study on sodium borohydride' -- subject(s): Sodium borohydride
Sodium borohydride
-1.24 v
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sodium borohydride and ethanol
Phenol is an acid while sodium hydroxide a base so it is acid base reaction forming the salt sodium phenoxide and water. C6H5-OH + NaOH = C6H5-ONa + H2O
We know NaBH4 as sodium borohydride.
There is no reaction between phenol and sodium carbonate