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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.
On mixing acetone and chloroform, a reduction in total volume occurs. What kind of deviations from ideal behavior for solutions is given in this case and why?
Mechanism of reduction (b)
what are the applications of coulumetry ?
Q. What Numerical prefixes indicate in ligands? In any complex species, the ligands are quoted in alphabetical order, without regard to charge, before the name of the central m
H-C=CH-CH-c
The nature of bonding in graphite is: (1) Covalent (2) Ionic (3) Metallic (4) Coordinate Ans: Covalent
0.45 g of anhydrous oxalic acid is reacted with 50 ml of KMNO4 . Then normality of KMnO4 is??
How does crystallography help in study of crystal structure
Explain why nichrome and not copper is used as heating element whereas manganin is used as standard resistance? For heating elements, primary requirements are high melting poin
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