Draw the product formed when the reactant shown is hydrogenated with an excess of H, in the presence of the Lindlar catalyst H₂ (excess) Lindlar catalyst Click and drag to start drawing a structure. 'ㅁ x A :
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- Draw the structure of the product/s in each of the following reactions. CuBr NaNO2, HCI, H,O, 0°C (F) (G) Para-methyl- aniline KI CUCN OH- (H) (), (J) phenolapp.101edu.co Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. esc F1 CH3CH2CH2OH H2SO4 (cat), heat ☀ F2 80 F3 OH a F4 W Q F5 Atoms and P Draw or ta MacBook A C F66) For the following Syl reaction: Draw a full 3-step mechanism with electron flow, intermediates, and the final product(s). excess CH₂OH 45 °C
- Step 4a: Classify step. The target product is present, but the reaction is not over. The ethoxide ion has been regenerated. :0: :0: What is the key process in the next step of the mechanism? proton transfer formation of a o bond between nucleophile and electrophile loss of a leaving group carbocation rearrangement (e.g., methyl or hydride shift)What is(are) the major final product(s) formed during the following sequence of reactions? 01 11 V 1.0₂ 2. (CH₂)₂S C₂H₂O 2 identical molecules ||| =PPhy < IV орнаWhich reagent/catalyst would be expected to bring about the following conversion? OH CH;CH2CH,CH CH;CH2CH,C-H ÓCH, Ag(NH3)2" / OH CH3OH / H3O* (1) NaBH4 (2) H30* O HNO3 / H2SO4 O K2Cr207/ H2SO4
- The accepted mechanism for a rearrangement reaction is shown below. "Q Ph (1) (ii) Ph Ph HO™ fast Ph Ph HO O™ slow Ph aufae .Ar² LOH HO™ fast Draw a curly arrow mechanism for this transformation. Sketch an energy profile for this reaction, showing approximate relative energies for the reactants, intermediates, transition states, and products. HQ Ph (iii) When DO™ was used as the reagent, the rate of product formation was same as for HO™. Explain why this result shows that the third step is fast and cannot be rate-determining. Ph (iv) Write the predicted rate equation for this mechanism, and show how it was derived. (v) The starting diketone may have two different aryl groups, as shown below. Propose a ¹³℃ labelling experiment that would allow you to distinguish which of the two aryl groups had migrated in this situation. OH AR²0- Ar¹ C Capp.101edu.co Draw the product of the reaction shown below. Ignore inorganic byproducts. H2, Ni heat, pressure Drawing Q Benz CThe conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.
- The reaction in the box is missing a reagent/reactant... NCH3 NHCH3 Which of the following would you use to convert the starting material into the product in high yield? A) An oxidation reagent such as H2CrO4 B) A base such as NaOH/H20 C) An acid such as H2SO4 D) A reduction agent such as NABH4 A В C O Da) b) - Fill in the reagents above/below the arrow in the following reactions. c) CN F CO₂H OH Хон4:15 ← OG Question 14 of 19 HgSO4, H₂O Draw the major product for this reaction. Ignore inorganic byproducts. H₂SO4 Select to Draw lll 52% > Submit