7. Provide a detailed mechanism for the reaction 2,2-dimethylcyclohexanol with phosphoric acid. Give the major product...
7. Provide a detailed mechanism for the reaction 2,2-dimethylcyclohexanol with phosphoric acid. Give the major product and do not forget the charges and arrows. (4 pts.)
6. A sample of 9.0 mL of cyclohexanol was mixed with 2.0 ml of 85% phosphoric acid and heated. The reaction yielded 4.0 mL of cyclohexene. Calculate percent yield for this reaction. (3 pts.) 7. Provide a detailed mechanism for the reaction 2,2-dimethylcyclohexanol with phosphoric acid. Give the major product and do not forget the charges and arrows. (4 pts.)
5. A common observation test to confirm the presence of an alkene (or unsaturation, in general) is the bromine test. a. What was the observation in the bromine test that allowed you to conclude an alkene was present? (3 pts.) b. Write the equation for the reaction between the major alkene produced and bromine. Be sure to show the correct stereochemistry in the product. (3 pts.) 6. A sample of 9.0 mL of cyclohexanol was mixed with 2.0 ml of...
Acid-catalyzed dehydration of 2,2-dimethylcyclohexanol yields 1,2-dimethylcyclohexene as one of the major products. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. ОН CH: CH3
Predict the major product of the acid-catalyzed dehydration of 2,2-dimethyl-1-hexanol. Then propose a mechanism with curved arrows of this reaction. 20) Predict the major product of the acid-catalyzed dehydration of 2.2-dimethyl-1-hexanol. Then propose a mechanism with curved arrows of this reaction. H2SO4 LOH heat
Devise a detailed mechanism for formation of the major product of the elimination reaction below. Draw curved arrows to show electron reorganization for the mechanism step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Devise a detailed mechanism for formation of the major product of the elimination reaction below. Draw curved arrows to show electron reorganization for the mechanism step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Devise a...
Provide the major organic product AND show the detailed, stepwise mechanism for the following reaction. Use curved arrows to show to complex AICI For the toolbar, press ALT F10 PC) O ALT.FN.F10 (Mac) Τ Τ ΤΤ Paragraph Arla 3 (120) X DOO T'T OS: Mashups - 1
22) Provide the major organic product of the reaction shown below. ( ( | 4 | | | H. 23) Provide a detailed, stepwise mechanism for the acid-catalyzed condensation reaction between benzaldehyde and methylamine. 24) Provide the major organic product of the following reaction. H2NNH, H (cat.)
Acid-catalyzed dehydration of 2, 2-dimethylcyclohexanol yields 1, 2-dimethylcyclohexene as one of the major products. Write complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures Consider the Grignard reaction below to answer the following questions The electrophile in this reaction is: The nucleophile in this reaction is: The alcohol product can be classified as 1'' alcohol 2'' alcohol 3'' alcohol 4'' alcohol Write the mechanism for the above reaction
Question 9 Provide the major organic product AND show the detailed, stepwise mechanism for the following reaction. Use curved arrows to show the flow of electrons. но NAOH Τ Τ Τ Arial • 3 (12pt) • T 111