Problem 26 of 34 Submit Curved arrows are used to illustrate the flow of electrons. Follow the arrows to predict the intermediate and product of ronction Includo
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- Chemistry Give the major product of the following reactions with the appropriate stereochemistry and regiochemistry 1. CH3 Compound A m. m. 1. Compound A; 2. dil. HCI CI Br n. 1. Compound A; 2. dil. HC1 Ph 0. 1. Compound A; 2. dil. HCI O2N.Draw the structure of the expected major organic product for each of the following five questions. Specify stereochemistry clearly, if relevant. А. Br2 aq. HBr H;CCO,H В. H;C° a.) LDA b.) PhSeBr c.) H,O2 8.50 x 11.00 inFor each of the following reactions, provide the missing starting material, reagent, and/or product. If more than one product can be formed, provide the major product. If no reaction occurs, write NR. ROOR HI 2. 3. он -0 Brz, H20 4. 5. HSO. (cold, conc.) HO;SO
- w how enols, enolate ions, andenamines act as nucleophiles. Predictthe products of their reactions withhalogens, alkyl halides, and otherelectrophiles. Show how they areuseful in synthesis.ences] Use the References to access important values if needed for this question. Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. oxidation CH,CH,SH reduction • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. C. opy aate Pre ChemDoodle"3. Predict products stereochemistry and mechanisms of the following reactions. .CO2H N. H (cat.) Ph N° A = .CO2R + A ? Ph Et solvent (i) (ii) (iii)
- A compound X is bitter in taste. It is a component of washing powder& reacts withdil. HCI to produce brisk effervescence dur to colourless, odourless gas Y wich turns lime water milky due to formation of Z. When excs of CO2is passed, ilkinessdisappears due to formation of P. Identify X, Y, And Z & P.3) wite down the open structures of A, B, C and D wfth the reactions the Tyn thes is D, scheme showing given in synthesis the of trust. of pheromone H-CミC- H 1) NANH2 l18quid NHg -78°C. 2) 1- bromo-5-methyl hexone 3(Cg Hgb) 1) NANH2//iquid NHs/-78 °C A (CaHi6) 2) 1-bromodecane P-2 (Nez B)/He . cicuHu) CiHg Cog H D(Cig H3pO) 19 19 CS CamScanner ile tarandı(2) Draw Suve the to products specify 1)BH 3 2) HzOz, H2O, оно of the sterco chemistry 1) Hg (0AC)₂, H₂0 2) Na BH4 H+ 1 H ₂0 H₂, Rancy Ni below, making where applicable. reactions
- 29. Select the structure(s) for the starting material(s), of the following reaction. Showing all relevant stereochemistry. m-chloroperoxybenzoic acid CH₂Cl₂, it H₂CH₂C.-C-C- H₂C H CH3[References] Use the References to access important values if needed for this question. Draw the structure of the organic product that is expected when the following compound is treated with concentrated H,SO4. CH3 CH2CCH2CH3 tosH heat HO. • You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ed P. opy aste C. CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and1) 1544565- NH₂ 2) CI of & 7) 8) reagents used: FeCl3/Cl₂ HNO3/H₂SO4 MeCI/AICI3 ACCI/Et₂N SO3/H₂SO4 Pd/C, H₂ NaOH H₂SO4/heat ACCI= CI [Choose ]