Predict the products and provide a detailed mechanism showing their formation. 3. i Кон 2
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows to indicate the movement of electrons. (a) (b) КОН (c) Note that formation of 4- or 7-membered rings is disfavored. Hiyo KOH acidie workup 2. An interesting problem that involves a bit of review (imines and Grignard chemistry) and application of what you previously learned to a new reaction: The Carbon of an imine functional group (i.e. R.C-NR) is sufficiently electron deficient to be...
3) (3 Points) Predict the product for the following reaction and draw the detailed stepwise mechanism for the following formation of the product showing all intermediates at each step. Br 1) xs NaNH2 2) H2O
2. Write the detailed mechanism for the formation of each of the products in the given reactions. Draw the structure(s) of the possible stereoisomer(s) for each of the products. OH OH HO+ (8pts) .chechem „ .8.8 НСІ
1. predict the major products.
2. draw detailed arrow mechanism.
1. Predict the major product of the reaction. Clearly indicate stercochemistry, if necessary На Lindlarca Me hexanes 2. Provide reagents to achieve the shown multi-step transformations (6 pts)
2. Write the detailed mechanism for the formation of each of the products ition of each of the products in the given Ons. Draw the structure(s) of the possible stereoisomer(s) for each of the products. OH Hot ism.
Provide a detailed, stepwise mechanism explaining the
formation of each product of the reaction.
30) Provide a detailed, stepwise mechanism explaining the formation of each product of the reaction below. OCH CHIOH heat Осн
predict the product for the following reaction and draw the
detailed stepwise mechanism for the following formation of the
product showing all intermediates at each step.
Br 1) xs NaNH2 2) H20
predict the product for the following reaction and draw the
detailed stepwise mechanism for the following formation of the
product showing all intermediates at each step.
Br 1) xs NaNH2 2) H20
provide a complete detailed mechanism for one side of the
reaction shown below
42. Provide a complete, detailed mechanism for one side of the reaction shown below. (10 pts). What is the type of mechanism? 1) КОН Br-
help! chemistry predict the products and mechanism!
the Product. Provide the stable organic product(s) for the reactions below. predict the Pro 1. Mgº, CH,CH,OCH,CH 2. CO (9) 3. H,O, HCI MgBr (X) 2. H,0,HCI 1. K Cr2O, H,SO, H,0 2. CH, MgBr (1 eq.) 3. H2O, HCI 1. Mgº, CH,CH,OCHCH 2. H20, HCI echanism. The following Grignard reaction has been observed to yield products A and B. MgCI THF-70 C 2. HCI, H20 0. Org. Chem. 1980, 45, 4952-4954. https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01430)...