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HW 5 1. Draw all possible products for the base catalyzed reaction of ethanal and propanal....
#4 is asking for a potential path to synthesize from the listed starting material to the final product. Including all reagents used and intermediary steps. The chapter this was assigned with is enolate anions & amines. 1. Draw all possible products for the base catalyzed reaction of ethanal and propanal. Indicate the new bond formed. (Full: all possible products and correct ID of new bond, partial: 75% of possible products) 2. Draw and label the kinetic and thermodynamic products for...
5. Draw the intermediates and final product for the following synthesis (Full: all products correct with no more than 1 minor error, partial: 3 out of 4 correct with no more than 1 minor error) Mg, Et,0 Br 1, CO, 2. H, H20 SOCI NH2
AT&T O D Jul 13% 18:43 PM Х HW 4.pdf Using the HNMR spectrum and molecular formula for the product, determine the structure. Complete the synthesis using an organometallic reagent and an aldehyde or ketone (Full: correct synthesis and HNMR assignment, partial correct NMR assignments) CHO Reagents for Synthesis 5 4 3 2 1 PPM 4.2 ppm, 1H, s 3.2 ppm, 1H,1 1.92 ppm, 2H, m 0.98 ppm, 12H, d 2. Using the HNMR data and molecular formulas, determine the...
1. Consider the following reaction: H-Bs A. Draw the mechanism of the reaction to predict all the possible stereochemical products of the reaction. Show all electron flows using the curved arrows. (1) Does the reaction produce a meso compound? Explain. Justify with relevant structures to get full credit. B. Design the following synthesis. To get full credit, you will discuss the rationale or justification for each step and reagents you decide to use. Refer to the video presentation in Lesson...
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...
PLEASE ANSWER ALL A-G, will give thumbs up!! FOR A, just need explanation why reaction occurs at C2 position rather than C3, already have mechanism drawn... PLEASE EXPLAIN OR AT LEAST JUST ANSWER ALL ASAP, BEFORE TOMORROW!! 10. Furan, an aromatic heterocycle, is capable of undergoing electrophilic aromatic substitution. When furan is treated with an acid chloride in the presence of a Lewis acid, Friedel-Crafts acylation occurs in which the electrophile is installed exclusively at the C2 position. Provide...