c) 1. NaNH 2. 1-bromobutane 3. H₂, Lindlar 4. MCPBA Skeletal Structure The reaction above produces two enantiomers. Show the Perspective Formulas of each
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- What are the chemical structure of me сиз сиз (excess] following musing compocents Brz. mono substituted MAHAA 2 G3 77 excess KM 12 छाट reduction E2 Reduction (mild pond) NaBH3 CH 3 Mg Br HLOH H E3 HOW Hyle. bor. Holt aid. H3 oxymer/ demo. H2 Three compounds A, B, and C all have the formula C6H10. All three compounds rapidly decolorize bromine in CC14; all three are soluble in cold concentrated sulfuric acid. Compound A has an absorption in its IR spectrum at about 3300 cm, but compounds B and C do not. Compounds A and B both yield hexane when they are treated with excess hydrogen in the presence of a platinum catalyst. Under these conditions C absorbs only one molar equivalent of hydrogen and gives a product with the formula C6H12. When A is oxidized with hot basic potassium permanganate and the resulting solution acidified, the only organic product that can be isolated is CH3(CH2) 3CO₂H. Similar oxidation of B gives only CH3CH2CO₂H, and similar treatment of C gives only HO₂C(CH2)…I need an explanation on this problem.First, we make sure we have isomers by performing the steps in Table I. Then, we go on to determine what kind of isomers we have. Classify the structures in Task 2 as different, identical, structural isomers (name type), enantiomers or diastereomers. Task 2 (Complete the task and discuss your answers on the discussion forum): 1 CH3CH₂CH₂C1 4 and CH3CHCICH3 Br -Br and ||| Br مکمل گیا میں Amud .Br. of and Br 2 5 Br Br and CH3CH2CH2CH2CH3 and CH3CHCH3 CH3 Br 3 6 Br and Br Br Br
- 4.(a). Draw the structures of (i) cis-1,4-Dibromocyclohexane and (ii) trans-1,4- Dibromocyclohexane. 4(b). Draw the most stable conformers of (i) cis-1,4-Dibromocyclohexane and (ii) trans-1,4-Dibromocyclohexane. 4(c)Which is more stable? (i) cis-1,4-Dibromocyclohexane or (ii) trans-1,4- Dibromolcyclohexane. Explain the reason for your choice.Only typed solutionA2.
- Show in each of the pairs below whether the two structures are structural isomers, stereoisomers, or different conformations of the same compound.4.) For each of the following pairs, give the relationship between the two compounds. You many ignore conformational isomerism here, and any conformers may be considered to be identical compounds. H H. a. H H H. H F F CH, b. он CH3 он c. CH, он он CH3 d. CHs CH3 CH, CH3 CH, .CH2 Br H. H. Br CH3 CH3 Br Br f. CH, H. CH3 он H. H Br Br H. OH 2C5H8 has two elements of unsaturation (right?), which may indicate the presence of either double bonds or triple bonds or rings. Show all the possible structures