Draw the product formed when the reactant shown is hydrogenated with an excess of H, in the presence of the Lindlar catalyst H₂ (excess) Lindlar catalyst Click and drag to start drawing a structure. 'ㅁ x A :
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- app.101edu.co Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. esc F1 CH3CH2CH2OH H2SO4 (cat), heat ☀ F2 80 F3 OH a F4 W Q F5 Atoms and P Draw or ta MacBook A C F68:16 NOO ← Question 11 of 27 ||| Choose the reagent(s) that would be most likely to complete this reaction. I ■ I I I I ■ ■ ■ RCO3H > O Submit HEE | 34% I I ■ I I I I I I I ОН r027 In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg 1) because bromide is a better leaving group than acetate. +
- The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"Draw the product of the reaction..g.(53) For the following is a 3-step synthesis problem, you are given: the Starting Material and the Product; a scheme of the expected conditions/intermediates and a list of 21 possible conditions and intermediates. Put the correct conditions/intermediates in the correct order to achieve this transformation.
- Rank the following esters from most reactive to least reactive in the first slow step of a nucleophilic acyl substitution reaction (formation of the tetrahedral intermediate): Rank the same esters from most reactive to least reactive in the second slow step of a nucleophilic acyl substitution reaction (collapse of the tetrahedral intermediate).The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.None
- app.101edu.co Draw the product of the reaction shown below. Ignore inorganic byproducts. H2, Ni heat, pressure Drawing Q Benz C(67) For the following is a 3-step synthesis problem, you are given: the Starting Material and the Product; a scheme of the expected conditions/intermediates and a list of 21 possible conditions and intermediates. Put the correct conditions/intermediates in the correct order to achieve this transformation.(63) For the following is a 3-step synthesis problem, you are given: the Starting Material and the Product; a scheme of the expected conditions/intermediates and a list of 21 possible conditions and intermediates. Put the correct conditions/intermediates in the correct order to achieve this transformation.