Draw the complete arrow pushing mechanism for the base-catalyzed keto/en the following compound. Label the reactant and final product as keto or enol below each structuure. Circle the most stable tautomeric form. OH NaOH H2O

Q: Give the mechanisim? Ho

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw a stepwise, detailed mechanism for the following reaction. но H+ CHO

A: At first the OH absorbs a proton turning itself into a good leaving group and then the double bond…

Q: NH2

A: Naphthalene, on reaction with concentrated H2SO4 at 1600C gives 2-naphthalene sulfonic acid. On…

Q: OH H3O* LOH

A: This mechanism is an example of neighboring group participation.

Q: CI NaH A

A: -> NaH is base hence, it can abstract most acidic hydrogen from given molecule.-> In presence…

Q: 4. Draw the keto tautomer of each of the following enols: OH он

A:

Q: OH 1:1 product H20

A: Ethylene glycol reacts with ketone to form ketal.

Q: Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is…

A: In the given question we have to predict the product and identify the type of reaction mechanism.…

Q: 2. Draw in the space below the acetal formed in the following reaction. (include all products)…

A: Hemiacetal and Acetal formation:

Q: Draw the enol form of the following ketone

A: First, let's discuss the enols. The enols are the type of reactive intermediate that has an alcohol…

Q: Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products…

A:

Q: Draw the mechanism for the following reaction. 0 EtOH, HCI

A: Step 1:This reaction is the nucleophilic substitution reaction of carbonyl compound,at first…

Q: 4) Answer the following questions about aldehydes and ketones ( a. Draw the curved arrow mechanism…

A:

Q: what is the enamine that will be formed from the below

A: Given is organic reaction. The given starting compound contains two functional groups imine and…

Q: Draw a stepwise mechanism for the following reaction, one step in the synthesis of the…

A: Protonation of oxygen atom takes place in the presence of acid H3O+ Hydrogen atom migrates to…

Q: Draw the arrow-pushing mechanism of the following tautomerization:

A: Draw the arrow pushing mechanism for the given tautomerization.

Q: Draw compounds B and C from the following reaction scheme. excess CH3I Ag20, H20 heat A B

A: In presence of excess of CH3I followed by oxidation by silver oxide, amines undergo Hoffmann…

Q: ОН H₂SO4 H2O, д

A: Beta keto acid is generally unstable substrate. It undergoes decarboxylation or it losses the…

Q: (v) Ethanal reacts with HBr and the resulting product is dehydrated

A: Aldehydes and ketones undergo nucleophilic attack because the oxygen of the carbonyl carbon is more…