ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
10th Edition
ISBN: 9781259972348
Author: Carey
Publisher: MCG CUSTOM
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Question
Chapter 23, Problem 24P
Interpretation Introduction
Interpretation:
The synthetic steps involved in the given retrosynthetic analysis are to be stated.
Concept introduction:
Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.
The compounds that possess the same functional groups will show similar reactions and characteristics features.
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Provide a retrosynthetic analysis and forward synthesis for the compound shown below.
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Chapter 23 Solutions
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
Ch. 23.1 - Prob. 1PCh. 23.3 - Problem 23.2 One of the hydroxybenzoic acids is...Ch. 23.4 - Prob. 3PCh. 23.5 - Prob. 4PCh. 23.6 - Problem 23.5 The compound shown was required for...Ch. 23.8 - Prob. 6PCh. 23.8 - Prob. 7PCh. 23.9 - Prob. 8PCh. 23.9 - Prob. 9PCh. 23.10 - Prob. 10P
Ch. 23.12 - Prob. 11PCh. 23 - The IUPAC rules permit the use of common names for...Ch. 23 - Prob. 13PCh. 23 - Prob. 14PCh. 23 - Prob. 15PCh. 23 - Prob. 16PCh. 23 - Prob. 17PCh. 23 - Prob. 18PCh. 23 - Prob. 19PCh. 23 - Prob. 20PCh. 23 - Prob. 21PCh. 23 - Prob. 22PCh. 23 - Prob. 23PCh. 23 - Prob. 24PCh. 23 - Prob. 25PCh. 23 - Prob. 26PCh. 23 - Choose the reaction in each of the following pairs...Ch. 23 - Pentafluorophenol is readily prepared by heating...Ch. 23 - Prob. 29PCh. 23 - Treatment of p-hydroxybenzoic acid with aqueous...Ch. 23 - Prob. 31PCh. 23 - Prob. 32PCh. 23 - Treatment of 2,4,6-tri-tert-butylphenol with...Ch. 23 - Prob. 34PCh. 23 - Prob. 35PCh. 23 - Prob. 36DSPCh. 23 - Prob. 37DSPCh. 23 - Prob. 38DSPCh. 23 - Prob. 39DSP
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- Please perform a retrosynthetic analysis showing all the steps and reagents involved.arrow_forwardIndicate the reagents and conditions to perform the following transformations.arrow_forwardUsing the disconnection approach propose a reasonable retrosynthetic route to accomplish the following chemical transformation. Include both the corresponding analysis and synthesis steps in sequential order.arrow_forward
- Provide a reasonable mechanism for these reactions. I suggest numbering your atoms. Assume aqueous work up to obtain neutral products.arrow_forward5. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps, best yields and best selectivity will get maximum marks. Me,SiQarrow_forwardretrosynthetic analysis and synthesus please explain with lots of detailarrow_forward
- b) Design a synthetic scheme using the reagents given for the following two reactions. All reagents are used for each reaction scheme and in each case, a reagent can be used more than once. Take the necessary time to complete this question. i) ii) 2 eq. 2 eq. H₂/ Lindlar's catalyst Br₂/CH₂Cl₂ lo 오오 H NaH H₂O+/H₂O H₂/Lindlar's catalyst PCC/CH₂Cl₂ NaH i H3O+/H₂O CH₂Brarrow_forwardSeveral reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.arrow_forwardProvide a reagent that will complete the transformations.arrow_forward
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