1. (15 p t) Complete the following reaction of saponification and show the mechanism
Show the products and complete mechanism for the following
reaction:
1. Show the product(s) and complete mechanism for the following reaction: H20+, H,O -CH₃
For the following saponification reaction, propose a mechanism.
Provide the structures of the three intermediates and two
products.
CH2CH2CH.COOCH CH3 + NaOH HO Intermediate 1 Intermediate(s) 2
Please show complete stepwise mechanism
Draw a stepwise mechanism for the following reaction [1] LIAIH4 CH2COCI → CH2CH2OH [2] H20
may you do this question and show the reaction mechanism
1) Complete the following reaction sequence: indicate regiochemical/stereochemical details as relevant i) Br, hv ii) C,H,ONa/C,H,OH, heat iii) HBr, peroxides iv) NaCN show product and mechanism
Provide a complete mechanism for the following reaction. 1 t-BuOH (1 eqv) 2. CH3CH2Br
Experiment #6: Saponification of Wintergreen Oil 1.) Draw a reaction mechanism for the conversion of wintergreen oil into salicylic acid. 2. ) If you wanted to take an IR spectrum to confirm that the reaction worked, what would you look for in the spectrum? 3.) It is also possible to hydrolyze an ester under acidic conditions. Draw a mechanism for the acid-catalyzed conversion of wintergreen oil to salicylic acid.
Mechanism #1. Suggest a mechanism for the following reaction and propose a practical method for driving the equilibrium to the right. obr. wown in boven TOCH + CH (CH),OH b(CH2-CH3 + CHOH Mechanism #2. The hydrolysis of esters using base (typically NaOH) is termed "saponification", and is often used to make soaps. Propose a mechanism for the saponification reaction shown below. Remember, hydroxide is a strong nucleophile. & non ha and
Saponification of
triglycerides
II. Saponification of triglycerides 1. Draw the reaction for the saponification of a triglyceride with NaOH that contains palmitic acid, stearic acid and linoleic acid:
Organic Chemistry
Complete the following mechanism. (Hint: P , AN , D , T )
Mechanism: Hydrolysis of a nitrile (ACIDIC conditions) 0. 0 HH HH I-o: EN: HH I-O: HH :0: HH
this is matlab..
updated, this is not matlab.
2. Saponification batch reactor. In a saponification reaction that takes place in a batch reactor, ester propargyl acetate (A) reacts with a base (B), which can be monitored using a conductivity meter. The conductivity, X(t) can be related to the fraction of base converted to a product, where: Fraction converted = CBt/CBo = [X(t) - X(0) [X(0) - X(0)] The table below shows the changing conductivity when 0.2873 M ester is reacted...