For each of the following, determine how the given product could be made from the given reactant. Show a retrosynthetic analysis then provide the synthetic pathway. a) H HO متھ تھا. (b)
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retrosynthetic analysis then provide the synthetic pathway.
a)
H
HO
متھ تھا.
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- 6) Which is the organic product for the following reaction? (a) (b) (c) (d) сон COOH ОН ОН COOH COOH KMnO4 H2OComplete the following syntheses – they may be two- or three-step processes. Include any necessary catalysts or reaction conditions. b) Prepare ethanoic acid from etheneChlorination of 2-butanone yields two isomeric products, each having the molecular formula C4H7ClO. (a) What are these two compounds? (b) Write structural formulas for the enol intermediates that lead to each of these compounds. (c) Using curved arrows, show the flow of electrons in the reaction of each of the enols with Cl2.
- Write the reagent or draw structures of the starting material or organic product(s) in the following reactions. If more than one product is formed, identify the major product where possible. (a) (b) HO OH OH H2SO4 ? Cl₂ ? FeCl3Complete the following syntheses – they may be two- or three-step processes. Include any necessary catalysts or reaction conditions. c) Prepare methyl ethanoate from ethanol and methanolIdentify which of the statements is/are correct. (i) The molecular formula of the smallest aldehyde is C3H6O, and that of the smallest ketone is also C3H6O. (j) The molecular formula of the smallest carboxylic acid is C2H4O2.
- [10] 10] Q1. Do the following conversions as directed. Write the complete reaction equation. (a) Benzaldehyde to Benzoic Acid. (b) Propanal to 1-propanal (c) Cyclohexanone to Cyclohexanol (d) Acetaldehyde to Ethyl alcohol (e) Acetone to Iso-propyl alcoholWrite structural formulas for the products formed in each of the following reactions, and categorize the type of reaction involved (a) CH3CH2CHO + (O) → (b) CH3CH=CH2 + HBr →(a) Draw the three isomers of benzenedicarboxylic acid.(b) The isomers have melting points of 210 °C, 343 °C, and 427 °C. Nitration of the isomers at all possible positions was once used to determine their structures. The isomer that melts at 210 °C gives two mononitro isomers. The isomer that melts at 343 °C gives three mononitro isomers. The isomer that melts at 427 °C gives only one mononitro isomer. Show which isomer has which melting point.
- Use the symbol (V) to indicate a positive reaction and the symbol (X) to indicate a negative reaction and a () if a test was not performed in the shaded columns. Don't forget to write the number of your unknown underneath where it says number! IDENTIFICATION OF A CARBONYL COMPOUND (GROUP I) Unknowns Number Number methyl ketone Test Aldehyde ketone DNP Fehling's Tollen's X lodoform X Therefore, unknown number is IDENTIFICATION OF ALCOHOL (GROUP II) Unknown Primary alcohol Secondary Tertiary alcohol number: alcohol Test Lucas (in ~5 mins) (immediately) Bordwell - Wellman Therefore, unknown number is > x x >Provide the common name for (a). Draw the structure for (b). Place you answers in the boxes provided.Dimethyl disulfide, CH,S–SCH3, found in the vaginal secretions of female hamsters, acts as a sexual attractant for the male hamster. Write an equation for its synthesis from methanethiol.
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