Q: 5. Design a synthesis of the target molecule from the starting material shown. of ОН
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Q: reagents in the correct order for the synthesis of the target molecule?
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Q: Show the reagents and the coupling partner that must be used in the above synthetic scheme.
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Q: With an example describe mechanistically how an extraction is carried out acid-base.
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Q: 1. Using retrosynthetic analysis, design a synthesis of the following target. HO Br Target
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A: IMPORTANT POINTS: In this type of question where precursor is asked ,here hypothetical hit and…
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Q: NH2 NH2 CI
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Q: 8. Design a synthesis of the target molecule from the starting material shown. ОН "ОН
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Q: 1. BH3 THF 2. H₂O2/NaOH/H₂O ●
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Q: Make a retrosynthetic analysis to design a synthesis plan. It should be ay least 2 steps synthesis
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Q: 3) Design a reasonable synthesis for the following transformation. = trort + B.
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A:
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- Draw the retrosynthetic analysis and synthesis for the following transformation.1. Using retrosynthetic analysis, design a synthesis of the following target. HO Br TargetA4 Express the retro synthesis scheme using the suggested starting material (SM) for the following target compound (TM). After performing the retro synthesis analysis, synthesize the target compound according to the analyzed scheme.
- Show the retrosynthetic analysis and forward synthesis of the following compounds. a. b. OH OH CHODesign a synthesis for the following reaction. More than one step may be required. If so, number separate steps. Show intermediate products to be considered for partial credit.Provide the retrosynthetic analysis and synthetic route for the following Compound.
- Perform a retrosynthetic analysis of the below including all necessary steps and reagents.Show the retrosynthetic analysis and forward synthesis of the following compounds. 1. د c 2. OCH35. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps, best yields and best selectivity will get maximum marks. Me,SiQ