Answer:
Explanation:
The reaction between dimethyl malonate which is an active methylene group with an (∝, β-unsaturated carbonyl compound) i.e methyl vinyl ketone is known as a Micheal Addition reaction. The reaction mechanism starts with the base attack on the β-carbon to remove the acidic ∝-hydrogens and form a carbanion. The carbanion formed(enolate ion) attacks the methyl vinyl ketone(i.e. a nucleophilic attack at the β-carbon) to give a Micheal addition product, this is followed by the protonation to give the neutral product.
Ba stays as Ba+2 and Cl stays as Cl-
Answer:
no
Explanation:
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If the dehydration reaction of an alcohol is successful. The changes would be seen in the IR spectrum for the product compared to the starting material are as,
- The O-H and C-O band is disappear from stating material
- The addition of a C-C double bond band in the product.
In dehydration reaction of alcohol ( O-H and C-O bond ) contain , the water molecule ( 
) is release from the reactant and C-C double bond is form which is known as alkene in the product .
The reactant and product have different structure. To determine the structure of the compound IR spectroscopy is used. In IR spectrum the peak corresponds to 3400-3600 cm is missing in the product of dehydration reaction of an alcohol. It means O-H band is disappear from stating material.
learn about IR SPECTRUM
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