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Reaction of conjugate addition
This reaction is a "conjugate addition" of cyanide ion on a cyclopropane. Notice that reaction at the least branched carbon of the cyclopropane happens and that the immediate product of ring opening is a very stable anion. Heating in acid protonates this anion, hydrolyzes the ester and nitrile groups, and decarboxylates the resulting β -keto acid.
#question.types of hydrocarbon found on oil contaminited site.
Assainment of liquefaction of gases in degree 2 nd sem
An ion has 18 electrons in the outermost shell, it is: (1) Cu + (2) Th 4+ (3) Cs + (4) K + Ans
Chemical properties of Cycloalkanes Cycloalkanes behave both such as alkenes and alkanes in their chemical properties. All cycloalkanes go through substitution reaction with ha
Highest melting point would be of: (1) He (2) CsCl (3) NH 3 (4) CHCl 3 Ans: CsCl
calomel construction and working
Prepare an assignment on the topic commercial cells
Which geometry does have Formaldehyde molecule The formaldehyde molecule has trigonal planar geometry. Therefore, both the H-C-H bond angle and the H-CAO bond angle are abou
What is difference between aluminium and beryllium?
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