Here is an abbreviated view of the molecule in the previous question with a large portion of the molecule abbreviated with the "R" carbon chain. R On + H;0 OH NH2 With your knowledge of Chem 131, you recognize the asterisked carbon on the lower portion of this molecule as a part of a functional group you are familiar with and how it is synthesized. Create a reaction scheme starting with the single molecule containing an aldehyde and an alcohol. Show the structure of the intermediate formed and the subsequent reaction with the additional alcohol to create the final product shown above (use the R abbreviation to indicate the rest of the molecule when needed). 1

How could one convert an aldehyde to a carboxylic acid? Group of answer choices-   Reduce the aldehyde with hydrogen gas (H2)   Oxidize the aldehyde using a mild oxidizing agent (such as permanganate).   Combust the aldehyde with molecular oxygen.   Use any of the above; each one would work OK.

Please help with this

Need help with these reaction questions. Include all products please.

The following chemical equation is for a substitution reaction, where the important atoms and groups involved have been highlighted for you: Hot. way + H HO O. H* ? + H-OH Use the information provided to predict the missing organic product and draw its structure in the drawing area below. Make sure to use the same skeletal ("line") style for the structure as the rest of the equation. Click and drag to start drawing a structure. X :0 S Om

Give the systematic (IUPAC) names for these molecules. Boononon cnolonongron. НаСНз CHОССH2СH2СНCHЗ CH3 phenyl propanoate |4-methyl pentane methanoat Incorrect. You mixed up the acyl and alkoxy portions of the molecule. Name the alkoxy part first, followed by the acyl part.

Pls it says it’s wrong

Q1 This question has two parts Part A and Part B. Part 1: Acetone can react with a base to give the enolate ion A, which can further react with another acetone molecule to give B. Upon quenching with water, B generates C, the final product of this reaction. :Base H20 A H3C H. H3C H. Acetone a) Draw the structure of A, B, and C b) Using curly arrows, draw the mechanism of the reaction between A and acetone to give compound B. What's the name of this reaction. - c) Draw the two resonance forms (A and D) of the enolate (A) generated by the deprotonation of the a-carbon on acetone and show the interconversion between the two using curly arrows: I Base H3C H A D H Acetone d) Knowing that the pka of the a-proton on acetone is 19, choose amongst the following bases those who will be able to remove the proton, given the pKa of their corresponding conjugated acids. H3C-C-H H H :Base H-Base + conjugate acid pka = 19 pКa 3 а, b, с, d a) Ammonia; pKa = 9.2 b) Sodium amide; pka = 38 c) Sodium…

Which of the following molecules is an acetal (Image added)

3.Complete the following Reaction. Include the IUPAC name of the product. [ OH + H₂C-CH₂CH₂-NH₂ a. H.S0₁ H50, +H₂C-OH- b. H,C—CH, + HO OH -CH₂