If u are referring to the carbocations of n-butyl, sec-butyl, and t-butyl, the most stable is the one that has the most alkyl groups attached to the positively charged carbon atom. In this case: - n-butyl has only 1 alkyl group attached - sec-butyl has 2 alkyl groups attached - t-butyl has 3 alkyl groups attached Therefore, t-butyl is the most stable carbocation
It comes from analcoholit's an ester
100mls of N-butyl, 3mls of glacial Acetic acid and 1.5grams of Ninhydrin.
The compound formed fromlithium and fluorine is named lithium fluoride. (As actually spelled, "litium" and "florine" are unknown.)
It is an alcohol 1-butanol or n-butyl alcohol, it is an organic liquid.
(CH3)3C- is t-butyl group. CH3CH2CH2CH2- is n-butyl group.
If u are referring to the carbocations of n-butyl, sec-butyl, and t-butyl, the most stable is the one that has the most alkyl groups attached to the positively charged carbon atom. In this case: - n-butyl has only 1 alkyl group attached - sec-butyl has 2 alkyl groups attached - t-butyl has 3 alkyl groups attached Therefore, t-butyl is the most stable carbocation
1-butene 2-butene di-n-butyl ether
n-butyl alcohol and propionic anhydride are used.
This is the butyl group often called the n-butyl group. this is an alkyl group. An example is n-butyl alcohol which is CH3 CH2 CH2 CH2OH
1.2676g/ml
nitrogen (N+) with 4 bondseach bonded to a butyl group (a 4 carbon hydrocarbon chain)iodine ion (I-) associates with N+ ionAKA tetrabutylammonium iodide
I think it depends on the circumstances. In my lab we used NaHCO3 to wash a mixture of n-butyl alcohol and n-butyl bromide. The NaHCO3 washed out the unwanted n-butyl alcohol in order to purify the n-butyl bromide component. In addition, the salt could be used to neutralize your organic layer.
C6h5coo(ch2)3ch3
It comes from analcoholit's an ester
101-102 C
Lithium + 1-chlorobutane ---> n-nuthyllithium + lithium chloride