Solution :-
In the first step alcoholic OH abstract the proton from the aulfuric acid
Then water molecules is removed and the carbocation is formed .
The secondary carbocation is less stable therefore the C-C bond shifted to fom a more stable carbocation that is tertiary carbocation.
Following image shows the steps on the reactio .
✅The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding...
The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding missing atoms and using lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in boxes 2 and 3. The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding missing atoms and using lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in boxes 2 and 3
The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding missing atoms and using lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in boxes 2 and 3.
The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding missing atoms and using lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in boxes 2 and 3.
Complete the mechanism for the acid-catalyzed racemization of the ketone below by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only). Complete the mechanism for the acid-catalyzed racemization of the ketone below by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only).
Complete the mechanism for the base-catalyzed opening of the epoxide below by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Complete the mechanism for the base-catalyzed opening of the epoxide below by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows.
Complete the mechanism for this cyclization reaction by drawing the missing intermediate structure and adding curved arrows. Show all lone pairs and arrows in each step.
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
10 Question (3 points) @ See page 920 Complete the mechanism for the intramolecular aldol reaction shown below. Add the missing curved arrow notation, lone pair electrons, and nonzero formal charges to all boxes. The reaction requires a base (e.g., NaOH) but we will ignore the Nat because it does not participate in the mechanism. Do not add any other reagents. :0— I Elcb Draw lone pairs, non-zero formal charges, and curved arrows to show how hydroxide reacts with the...
Draw the mechanism for the formation of the kinetic product of the reaction conditions shown by completing the following: Draw the mechanism for the formation of the kinetic product of the reaction conditions shown by completing the following: 1. In the first box, draw curved arrows to show the interaction of the two reactants. 2. In the second box, using the structures provided, add any lone pairs and nonzero formal charges, adjust the number of hydrogens on the three carbons...
Complete the mechanism for the base-catalyzed racemization of the chiral ketone below by adding any missing atoms, bonds (wedge/dash, too), charges, nonbonding electrons, and curved arrows (forward reaction only). This is what I tried, but the top 2 boxes were wrong: Complete the mechanism for the base-catalyzed racemization of the chiral ketone below by adding any missing atoms, bonds (wedge/dash, too), charges, nonbonding electrons, and curved arrows (forwarod reaction only). :OF enantiomer O Previous Give Up & View Solution e...