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Standard IX
Biology
Carbohydrates
39 What will ...
Question
39 What will be structure of 3,3-Di-tert-butyl -2,2,4,4-tetramethylpentane
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Q.
If
2
,
2
,
4
,
4
−
tetramethylpentane is subjected to free radical chlorination, how many different isomers are obtained on dichlorination?
Q.
Arrange the following compounds in the increasing order of their reactivity towards HCN.
I. Acetaldehyde
II. Acetone
III. Methyl-tert-butyl ketone
IV. Di-tert-butyl ketone
Q.
Given below are two statements labelled as Assertion (A) and Reason (R).
Assertion (A):
Di-tert-butyl ether cannot be prepared by Williamson's synthesis.
Reason (R):
tert-butylbromide on treatment with sodium tert-butoxide preferentially undergoes elimination to from iso-butylene and tert-butyl alcohol.
Q.
Give the structure and IUPAC name of Di-tert-butylamine.
Q.
What will be the major product obtained in the reaction between tert butyl chloride with sodium methoxide?
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