I react with ethanol how would I draw the product?

Give the IUPAC and common name for the following compounds. a. HO, b. но OH

Draw the principal organic product for the reaction of 2-bromohexane with lithium in diethyl ether, followed by formaldehyde in diethyl ether, and then followed by dilute acid. Click and drag to start drawing a structure. X A G P

What are the steps and reagents needed to synthesize this molecule?

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.

Answer all three parts plz. You are starting with three aryl bromides. They undergo a typical grignard reaction with magnesium metal and anhydrous ether (diethyl ether). Dry ice is then added to it and it is then cooled. Draw and label the names of the aryl carboxylic acids that will form for each. Part a) 4-bromonitrobenzene Part b) 4-bromotoluene Part c) 2-bromotoluene

What explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions? A. The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile B. The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile C. The oxygen of the carbonyl group can attack the carbon of the carbonyl group D. Only esters can undergo self-condensation reactions

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1) Draw the structures of the reaction products: Reaction 1 Reaction 2 Reaction 3 OH OH OH OH ii H* H* OH + H₂C-OH OH H* H₂C OH 2) According to your data for Reaction 1, which OH group reacted as the nucleophile: the OH of the phenol, or the OH of the carboxylic acid? Explain your answer using your data.

you want to synthesize butanoic acid you have propyl bromide, magnesium, and carbon dioxide. draw the reaction scheme - how would we design this reaction?