2-bromo-3,4-dimethylpentane is combined with t-butoxide. The product of this reaction is 3,4 dimethyl - 1- pentene.
The reaction of 2-bromo-3,4-dimethylpentane is combined with t-butoxide forms 2 alkene in the elimination reaction due to steric hindrance. The least stable alkene 3,4 dimethyl - 1- pentene is easy to make. the t-butoxide is (CH₃)₃CO⁻. The reaction involves in this reaction is E2 elimination reaction. This reaction involves the one step reaction. The product will also form that is 3,4 dimethyl - 2 - pentene. so the reaction involve Elimination reaction and the product due to steric hindrance is 3,4 dimethyl - 1- pentene
Thus, 2-bromo-3,4-dimethylpentane is combined with t-butoxide. The product of this reaction is 3,4 dimethyl - 1- pentene.
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Answer:
it identifies reducing sugars (monosaccharide's and some disaccharides), which have free ketone or aldehyde functional group
Explanation:
It turns from turquoise to yellow or orange when it reacts with reducing sugars.
Answer:- 2.39 mL are required.
Solution:- It's a dilution problem and to solve this type of problems we use the dilution equation:
Where, 
and 
are molarities of concentrated and diluted solutions and 
and 
are their respective volumes.
= 1.10M
= 5.00mM = 0.005M (since, mM stands for milli molar and M stands for molar. 1M = 1000mM)
= ?
= 525 mL
Let's plug in the given values in the formula:
So, 2.39 mL of 1.10M are needed to make 525 mL of 5.00mM solution.
High energy hope this helps
