S.4. Using all the benzene as given in the reaction below, show all the steps necessary...
3) Write the names of the molecules whose explicit structures are given below, according to the naming system. Write the open structures of the named compounds NH он a) CH3 соон NO2 b) ON -COOH -NOZ d) e) h) f) 2-Naphthoic acid g) 2,10-dimetilantras anisole i) o-cresol j) 3-aminopyridine 4) Using all the benzene as given in the reaction below, show all the steps necessary to synthesize the target compound, o-nitroaniline. Indicate what is the appropriate reagent in each step...
Benzene can be converted to 2,4,6-tribromoaniline in three reaction steps and two intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. Benzene can be converted to 2,4,6-tribromoaniline in three reaction steps and two intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis.
r each compound below, identify which position(s) is/are most likely to undergo an electrophilic aromatic substitution reaction? Circle the carbon that undergoes electrophilic substitution. (3) b. CH NO2 O2N What Wittig reagent and carbonyl compounds are used to synthesize the following compound? (2) c. (CH3CH2)2C-cHCHCH2CH3 Write the equations to convert benzene to the following compounds? Some conversions need more than one step. (10) 3. a. Toluene b. m-bromo nitrobenzene c. Benzene sulfonic acid d. Aniline e. Benzoic acid r each...
Give reagents necessary to synthesize the molecule below using the Stork enamine synthesis. Show all steps in detail.
Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. (All drop down menus have the same reagants). Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. Step 1 Step 2 Step 3 Step 4 Step 5 Br Br Br Reagents...
Design a synthesis of n-propylbenzene from benzene. Hint: A one-step synthesis using CH,CH CH Br and AlBr yields a large amount of isopropylbenzene. 4. 5. Design a high-yield synthesis of each target starting from benzene NO2 NH2 NH2 H2N CI CI target target target target
51. Make the following compound from the starting reagent. Show all the steps, reagents involved and the intermediate products. a. 7 بل mynd OH b. Synthesize the following molecule from benzene via a diazonium salt. Show all the reagents and the intermediate products. COOH OH c. Synthesize the following amine from the given alkyl halide in good yield. Show all the intermediates and reagents. CHE
What are the correct choices for the three steps? Benzene can be converted to 2, 4, 6-tnbromoamlme in three reaction steps and two intermediate compounds Select the appropriate reagent from the drop-down list for each step in this overall synthesis.
Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. Step 1=? Step 2=? Step 3=? Step 4=? Step 5=? Options for each step: Br2, R2O2 CH3Cl, AlCl3 CH3COCl, AlCl3 NaNO2, HCl HNO3, H2SO4 H3PO2 H3PO4 KMnO4 1) Sn, HCl; 2)OH- Br2 Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from...
Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. Reagents