--- alance refer to your Assin 8. Give the equation for each of the following syntheses...
Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organic reagent of TWO carbons or less: 4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. The synthesis should not take more than three or four reactions. At least one of the reactions should come from the aldehydes and ketones chapter. (6 pts) a) CO2H b)
12) Starting with hex-3-en-2-one, propose syntheses for the following compound the following (8 pts total): propose syntheses for the following compounds. For each synthesis, indicate op that needs to be done to add functional groun (ex: reduction: dehydration: Grignard, etc.) - include reagents required for the transformation (ex: NaBH, for carbonyl reduction, etc.) OH MY OH *Hint: refer to g. 11
oblem 10.47 ( 10 of 13 a alance each of the following neutralization eactions. Review | Constants 1 Periodic Table HCl(aq) + Zn(OH)2(8) → ZnCl2(aq) + H2O(l) Express your answer as a chemical equation. Identify all of the phases in your answer. That's not quite right. Please check your formatting and try again. No credit lost. Try again. Submit Previous Answers Request Answer Part B H,PO (aq) + KOH(aq) + K3PO.(aq) + H2O(1) Express your answer as a chemical equation....
5. Give the organic products of each of the following multistep syntheses. You are required to draw only the structures of the final products. Drawing the products of individual steps is optional and may be graded for partial marks. No mechanisms are required. 1.H20* 2. Na2Cr207, H2SO44 2 a) 3. PhMgBr 4. H2O 1. EtMgBr 2. H2O 3. Na2Cr207, H2SO4 (aq) 3. EtMgBr 4. H20 1. NaNH, 2. Mel 3. NaNH2 HCECH 4. Eti 5. Na, NH, 1. Mg /...
(48 pts, 4 pts each) Give an acceptable IUPAC name for the following compounds 1. CH b. coH CH C. OH DO d. ollal ol oun COOH е. Br f. CH2 Br CH-CH,-CH-CH2-CH- CH,-CN
3. Give the structures of the products of the following alkene syntheses and explain why these products are obtained. (15 marks) Ph a) a = Na, NH3 (1) t-BuOH, -78 °C NON NaOH Etus H Me Ph Me Br (major and minor products) MezSi Me NaOH c) Ph Et Me OH
3. Show efficient syntheses of each of the following from the indicated compound and any need organic or inorganic reagents. (50 pts) (a) 1-popene, from 1-bromopropane (b) 1-chloro-2-butanol, 1-bromobutane (c) 2-pentyne, from propyne (d) trans-1,2-dibromocyclohexane, from cyclohexanol (e) 2,3-hexanediol, from 2-hexene 3. Show efficient syntheses of each of the following from the indicated compound and any need organic or inorganic reagents. (50 pts) (a) 1-popene, from 1-bromopropane (b) 1-chloro-2-butanol, 1-bromobutane (c) 2-pentyne, from propyne (d) trans-1,2-dibromocyclohexane, from cyclohexanol (e) 2,3-hexanediol,...
Propose syntheses of each of the following compounds, from the given starting material and any other needed reagents. » O- CH2OH from O con b) CH3CCHz from CH3CH=CH2 ОН • OCHGHs from O-Br
8. Describe the best method for each of the following laboratory syntheses, given a single reactant. Include why you chose this method in your description. a) 1-butanol converted to butanal b) 1-butanol converted to butanoic acid c) 2-butanol converted to 2-butanone d) 2-butene-1-ol converted to 2-butenal e) 2-butene-1-ol converted to 2-butenoic acid f) 1-methylcyclohexanol converted to 2-methlycyclohexanone (this is a multi-reaction process)