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What simple characterization techniques can you say that your product is dibenzalacetone?
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- Why do you think the product undergoes favorable dehydration?Give the reagents and results/observation (ex. color) Test for aldehydesa. Schiff’s testb. Formalinc. Acetoned. Benzaldehydee. AcetophenonePerform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from the given starting material (on the right). (any reagents maybe used
- Draw the form of the following compound that will predominate at pH 10.This NMr and IR spectra show the product of an unknown grignard reaction to be 4-methoxy benzoic acid. Does this mean that the Grignard reagent is Methoxyphenylmagnesium bromide? Please include the complete mechanism in the explanation.what type of mechanisims is needed for this?
- What functional group cannot be present on the substrate when treating it with either an alkyllithium or Grignard reagent?Apply retrosynthetic analysis to identify all the practical combinations of Grignard reagent and aldehyde or ketone that will give the required target.Just one quick follow-up question. Would this reaction be considered an imine formation?