Interpret the 1H NMR spectrum of Indole-3-Carboxaldehyde

Using the 1H NMR complete the following table and draw the structure.

compare and construct the nucleophilic reactions of hcl with propanone, propanal and propan-1-0

write structural formulas for the products that form when propanal reacts with phenylhydrazine. draw a step by step mech

Which of the following functional groups are present in 2-hydroxy-1,2-diphenylethan1-one? Group of answer choices aldehyde mono-substituted phenyl alkene carboxylic acid nitro ketone amine ortho-disubstituted phenyl ether alkyl ester amide hydroxyl

The product of reaction between formaldehyde with 2-methyl propanal give 2,2-dimethyl-3-hydroxy propanal 2,2-dimethyl-3-hydroxy propanone 2,2-dimethyl-3-hydroxy propanoic acid 2,2-dimethyl-3-hydroxy propanol 4-phenyl-3-buten-2-one prepared from reaction between Benzaldehyde with acetic acid Benzaldehyde with acetaldehyde Benzaldehyde with formaldehyde Benzaldehyde with acetone Which predict product for reaction between heptane-6-one-1-al with sodium hydroxide * 1-(2-hydroxycyclopentyl) pentanone 1-(2-hydroxycyclopentyl) butanone 1-(2-hydroxycyclopentyl) ethanone 1-(2-hydroxycyclopentyl) propanone

As a method for the synthesis of cinnamaldehyde (3-phenyl-2-propenal), a chemist treated 3-phenyl-2-propen-1-ol with K2Cr2O7 in sulfuric acid. The product obtained from the reaction gave a signal at δ5 in its 13C NMR spectrum. Alternatively, when the chemist treated 3-phenyl-2-propen-1-ol with PCC in CH2Cl2, the 13C NMR spectrum of the product displayed a signal at δ193.8. (All other signals in the spectra of both compounds appeared at similar chemical shifts.) (a) Which reaction produced cinnamaldehyde? (b) What was the other product?