please show mechanism with arrow-notation 10.) Write the main product of the following reaction and explain...
10) Using the curved arrow notation, write a mechanism for the following reaction of an enamine with an alky halide. Br- 2C-O-CHCH, Du-CH₂ CH3
4 4) Write the reaction product and use the curved arrow notation to draw a mechanism that accounts for the formation of product upon oxymercuration/ reduction of cis-4-hexenoic acid in aqueous THF. (8 points) a) Write the reaction. 1) Hg(OAC), aq, THE 2) NaBH, aq. THE HO cis-4-hextenoic acid b) Write a mechanism.
Using the curved arrow notation, write a stepwise mechanism to rationalize the formation of each product in the following reaction (you may need the back of this sheet).
Show the mechanism for the following reaction and determine what the main product is. 10.) Show the mechanism for the following reaction and determine what the main product is. (5 points) 1.) H2N-NH2 2.) NaOH, H20
Please show detailed arrow-pushing mechanism. Best regards. C) Please provide the product of the following reaction and concisely explain why you get the observed constitutional isomer. Drawing the appropriate orbitals will really help to explain your answer. (2 points box, 4 points explanation, 6 points total section). 1 H O-Na H Mel
B. Using curved arrow notation, draw the reaction mechanism and predict the product the reaction below. Show all reaction intermediates and account for stereochemical requirements. [6 MARKS) EtOna / EtOH ? OTS Heat
10. What is the product of the following Diels-Alder reaction? Show the complete arrow pushing mechanism that accounts for the product. co Et heat CO,Et
Draw the structure of the product(s) and use arrow notation to show the mechanism of the reactions below a) NaOH C7H15N H2o b) 1) KOH ОН 2) CH3OCH2CI
1.2.3.4.5.6.7.8.Show the curved arrow mechanism for the reaction between ethoxide and methanol to give ethanol and the methoxide ion. 1st attempt Jual See Periodic Table See Hint OH-Ö: Add the missing curved arrow notation.The carbon-metal bond in organometallic Grignard reagents exhibits significant covalent character. However, we can treat these compounds as electron-rich carbanions because of the large difference in electronegativity between carbon and magnesium. These reagents are great to form carbon-carbon bonds but must be kept in an anhydrous environment...
Part III - Mechanism cont'd B. Using curved arrow notation, draw the reaction mechanism and predict the product the reaction below. Show all reaction intermediates and account for stereochemical requirements. [6 MARKS] or EtoNa / EtOH ? OTS Heat