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- Please help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank youAl₂(SO₄)₃ + 3Li --> 3Li₂SO₄ + 2Al Show the reactant and product.CH3 to Br- -H + Nal • product; Sy2 product of the reaction is : Аcetone H- -CH3 CH2 – CH3 CH3 CH3 CH3 CH3 it it -H H- -CH3 (d) -CH3 -H- (а) H• (Ъ) H- -CH3 -CH3 (с) H- CH -H- ČH2 – CH3 ČH2 – CH3 CH2 – CH3 CH2- CH3 2.
- 4. Protonation of alcohol A and subsequent loss of water, produces the intermediate B. CH3 CH; CH, CH, — с — сH, CH, CH;CH, - C- CH, CH; | OH A B (a) (i) Name alcohol A. (11) What type of species is intermediate B? (iii) Draw the structures of the two alkenes which can be formed from species B by removal of a proton. Label as C the alkene which shows geometrical isomerism. (b) The intermediate B is readily attacked by nucleophiles such as water. What is the essential feature of a nucleophile? (c) State what final colour you would see if alcohol A were warmed with acidified potassium dichromate(VI). Explain your answer. Colour Explanation . (ii) Draw two structural isomers of alcohol A which form branched chain ketones when heated with acidified potassium dichromate(VI), but which could not form alkene C on dehydration.Predict the product for the following reaction. H₂C A I and II HH3C xoxoxox B D IV E cis-1-bromo-3-methylcyclohexane ||| SH H₂C NASH III acetone Br H3C ||||SH IV H10. What is the major organic product generated in the reaction below? HO HO 40||!!!!!! (A) OH ...... (B) 1) 03 2) (CH3)2S HO O (C) H НО. (D)
- Draw the organic prouduct of the reaction with a) HBr b) Br2 c) H2, Pt/C d) O3; (CH3)2SPPh3, DIAD CH20H (A) THF mitsunobu H2N sreaction NH2 excess AGOH () (Ci3H20 INS) me I N-me mePredict the major products. C,H5-C-CH; а. 1/2 b. (CH;),CH-C-Ħ#", heat (CH),СH-C-Нт C,H5-CH2-C-Ħ с. d. C,Hs-C-CH; H" CaH-C-CH С,Н-С-СH е. f. CHs-C-CH;¬N#OH CH;-C= C-CHOTE gSO g. h. C,Hs-C-C,H5 H*
- Predict the product for the following reaction. Ш | ОН 0 ОН 1. DIBAH 2. H2O || IV I ОН ОН ОНreactions. Be sure to show any significant stereochemical details. (a) I. Nall. CS 2. CH,I 3. heat (b) 1. BULI, LICI 2.MeCu(CN)LI (c) CH, Zn-Cu CH,l,, ether (d) CH,CO,H LOET (e) Br Zn, THO.6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HO