4. Complete the solution of the exercise below by writing out the mechanism step by step...
Chem 322L Assignment 4 1. Classify each of the following alcohols as primary, secondary, or tertiary. нс Үсн, OH a) Hzc? H2C CH CH c) HO 2. Identify (Circle) and name the three functional groups in the following molecule. CO2H HOC 3. Provide the products of the following reactions. COOH + CHOCH.CH w a CH HO b) 4. Complete the solution of the exercise below by writing out the mechanism step by step. Tetrahedral intermediate 5. Give the structure of...
4. (5 pts) Draw a complete, step by step mechanism to account for the formation of following product. Draw all the resonance structures of the intermediate and indicate which one is the major resonance contributor. осна OCH3 Br2 FeBr3
Draw the two step mechanism for the nitration of bromobenze to give the para product. Draw the four major resonance contributers for the intermediate cation. Circle the resonance structure that is particularlt stable, and explain the reasoning.
Please try to show/explain every step!
22. Complete the following reactions by clearly writing out the products and state if the product is a water soluble molecule or not. (3 pts cach/15 pts total) HO NH,Br. H,804 HAPO, 200 °C HBE No peroxides CH,CH 23. Complete the following reactions and show the mechanism of how the reaction occurred. You must identify at least one nucleophile and one electrophile in cach mechanism that you draw. Only do ONE of the two...
How do I complete the mechanism and write out the
description?
4) Complete the mechanism for the reaction given below, then generate a description of the mechanism. Don't show the reaction or mechanism to your partner. OH CICI 1 equivalent
Show the complete mechanism for the reaction below. Label each step in the mechanism with the name of the elementary step. Her 0 ROOR Initiation Propagation Termination
If the Favorskii R of 2-chlorocyclohexanone is carried out using sodium ethoxide in ethanol, the product is ethyl cyclopentanecarboxylate, shown below. CI CH,CH2O Na The reaction procceds via a 5-step mechanism and can be formulated as follows. Step 1: Formation of an enolate ion 1 and ethanol. Step 2: An intramolecular alkylation reaction, with enolate ion I as the nucleophile, to yield a fused ring intermediate 2 and Cr. Step 3: Formation of a tetrahedral carbonyl addition intermediate 3 Step...
Write the complete step-wise arrow.pushing mechanism for reaction shown below. Show electron flow with arrows, and be sure to include all intermediate structures. You must be very detailed in your mechanism for full credit. H2SO4
Predict the major organic product of the following reaction and complete its mechanism below. 1) NaOEt/EtOH 2) CH3CH2CH2Br 3) dilute NaOH/heat 4) H30* 5) heat Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. :O O: :Br. CH3CH2OH Do not show curved arrows for this step. Added acid Dilute HH NaOH and heat hydrolyzes the ester. O: Na Br - H20, Na* O: 100-150 °C O:
what are the major products of the reaction below and give a
complete step by step of the reaction mechanism.
OH NaOH, water