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- acetone H3C, HO H3C OH The product of the following reaction is: A OH H3C OH C D OBDraw the structure of the products formed in the following reactions. a) CN H,0, H* CH3 он b) H3C- -CI + CH3 c) CH3 KMNO4, A, H,O" CH3 d) Br Mg, éther CO, H*What is the major organic product obtained from the following reaction? OH OH H,0 CH;CH,CH,CH,C=CH OH HgSO, H,SO, ÓH O 1 O 2 O 3 O 4
- Which compound is the dominant product in the reaction shown below? KMNO4 .COOH (A) H*/H,O (B) COOH .COOH (C) (D) HOOC HOOC Compound B Compound C Compound D Compound AIdentify the product(s) of the reaction below: -сон CHCI, KOIBU OHC A) CI CI OHC CH,COOH OHC ČH,COOH ci ci B) HOH2C CHCHOOH C) HH OHC CH2COOH OHC ČH,COOH HH D) H. OHC Снсноон What is the IUPAC name of the following compound? A) Butyl propanoate B) Propyl heptanoate C) Propyl butanoate O D) Heptanoic acidWhat reagents are required for the below conversion: O CH=CH CuLi مله O MgBr, ether ; CH=CH2 , H2O 1 (CH2=CH),CuLi ; H2O, HCl O MgBr ; H2O, HCI
- Name the following organic compound: CH3 S CH CH3 CH 0 CH, CH, 3-methylsulfide-2-ethoxy butane 2-ethoxy-3-methylthio butane O 3-ethoxy-2-methylthio butane O 2-methylsulfide-3-ethoxy butane O 2-ethoxy-3-methylsulfide butaneWhat is the organic product formed in the following reaction? C6H5-CH=CH-C-C6H5 ÷ (CH3CH2)2NH O C6H-CH-CH-C-C6H5 (CH3CH2)2N || III CH-CH, CH- (CH3CH2)2N -CH OH IV O-N(CH2CH3)2 C6H3-CH=CH-C-CH¸ CH-CH=CH-C-CHS (CH3CH₁₂N Select one: A. IV B. II OC. III D. I F1 10: - F2 80 F3 000 000 FAWhich of the following reactions are correct? Explain the answer. + H₂O + H₂O H₂SO4 H OH H OH
- 12 Write the IUPAC names for these compounds. O (a) CHO CHOH (c) | CHOH I CH₂OH OH (b) (d) CHO NH₂ OWhat alkene is needed to synthesize each 1,2-diol using [1] OsO4 followed by NaHSO3 in H2O; or [2] CH3CO3H followed by −OH in H2O?4. A student was asked to prepare an alkene X in high yield using any alcohol as starting material CH3 CH,-C -CH=CH, CH3 X He chose 3, 3-dimethylbutan-2-ol (XI) and carried out a dehydration reaction. He was however horrified to note that the only alkene obtained was XII. CH3 OH CH3 CH;-C=C-CH3 conc. H,SO4 CH-CH3 heat CH3 CH3 XI XII i) Explain what went wrong here, and why X could not be formed from 3, 3-dimethylbutan-2-ol. Use structures to help support your answer. ii) Give an equation to show a much better method for preparing X in high yield. 5. Analyze the following structure and write one combination for Grignard reagent and a carbonyl that would give rise to it. CH,-CH,-OH