1% 70- 60 50 9 30 20 10 of 4000 3490.50m-1 3500 307041cm-1 O 2-methylcyclohexanone O acetophenone O benzoyl chloride O benzyl acetate O butyrolactone O cyclopentanone O methyl benzoate O methyl propionate 3000 2500 1773 120m-1 cm-1 2000 1734.171 144981 120 2021 1595 22-1 1500 11741 1000 500

Q: At least three chemical reactions Methyl chavicol (estragole) C10H120 can undergo?

A: Methyl chavicol (also known as estragole) is an organic compound with the chemical formula C10H12O

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Q: 1% 80-₁ 70 60 50- 40 30 20 10 -07 4000 3490.50cm-1 O acetophenone 2-methylcyclohexanone 3500 benzoyl…

A:

Q: 102 100- 95 733.63cm-1, 96.21%T 90 1167.81h-l 92.47%T 69.96cm-1, 93.62%T 10 04cm-1, 89.79%T 85 28H…

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Q: What is the correct structure for N-butyl-butanamide? О IZ О H IN О O

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Q: Please check if the information below is correct. Specifically the aroma produced by the ester

A: To check if the information below is correct, Specifically the aroma produced by the ester:

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Q: c) cyclohexanecarboxamide d) benzoic propanoic anhydride e) octyl butanoate

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Q: 3 PPM 2 180 El-MS: 88.1 160 140 120 100 PPM 80 60 40 20 0

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A: Given,The pyranose is:

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Q: Provide the correct IUPAC name for the compound shown here. HS 2-methylpropan-2-thiol

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Q: ОН CH3 HO, OH CH3 H. Cortisol a) NaCN b) НзРО4 85% с) NaBH4 d) NaH е) NaOH

A: To check which reagent attack which functional group

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Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.