The compounds below are reactive with one another in a Diels-Alder reaction. Draw the resonance structure for each one that would help to indicate how they would align. 2nd attempt See Hint :N

Benzoic acid QUESTION 2 Which statement about the cyclopentadienyl radical is correct? O It is aromatic. It has a Hückel number of pi electrons. It is not aromatic. It has a completely filled bonding shell of six pi electrons. QUESTION 3 Click Save and Submit to save and submit. Click Save All Answers to save all answers.

In the box below each molecule write down the number of r-electrons. Circle all of the following molecules that would be aromatic, and underline all of the following molecules that would be anti- aromatic. 2) CS Scanned with CamScanner :0:

Determine which, if any, lone pairs are participating in aromaticity

Need to check answer 1.Borane (BH3) adds to alkenes to form an alkylborane. In the first box draw the mechanism arrows, and in the second box draw the correct product. Be sure to add lone pairs of electrons and nonzero formal charges to all species.

O Macmillan Learning Question 21 of 35 Draw the correct product for the Diels-Alder reaction. > + Select Dr

Give a clear handwritten answer with explanation

Can you please let me know theanswer and explain why that is the answer?? Thanks.

The reaction shown below yields a mixture of two Diels-Alder adducts. In the box below draw the structure of both products. Br Products

The reaction shown below yields a mixture of two Diels-Alder adducts. In the box below draw the structure of both products. Products