Draw structures for the organic products (A-G) that would form in the following reactions. Show stereochemistry where relevant! a) b) c) EC-CH3 H3C-CC 1) BH3 2) H₂O2, HO H₂ Lindlar catalyst B 1) KMnO4 2) Hydrolysis reaction is heated up A C + D
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- Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questionsA)What is the IUPAC name for Compound X?B)What type of reaction (s) is/are represented by (i) and (ii)?C)Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. D)Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed.E)Which of the compounds in the following pairs will occur in relatively higher yields and why?I)[1] and [2] II)[3] and [4]Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questions. –a. What is the IUPAC name for Compound X? b. What type of reaction (s) is/are represented by (i) and (ii)? c. Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. d. Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed.e. Which of the compounds in the following pairs will occur in relatively higher yields and why?i. [1] and [2] ii. [3] and [4]Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questions. A. What is the IUPAC name for Compound X? B. What type of reaction (s) is/are represented by (i) and (ii)? C. Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. D. Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed. E. Which of the compounds in the following pairs will occur in relatively higher yields and why? [1] and [2] [3] and [4] The attached image contains the scheme.
- A. For each reaction1) Provide the missing reagents/conditions or major organic products as appropriate2) Assign each reaction as Oxidation or Reduction unless otherwise directed3) Pay attention to stereochemistry including racemic mixtures unless specifiedA student in Ochem proposed the following synthesis. Explain the problem with this approach and provide the necessary reagents to convert halohydrin A to alkene B (more than one step is required) in addition provide the product after each step. Provide the mechanism and expected actual final product from the reaction of halohydrin A with LDAI need specific description of the compounds involved in the synthesis (functional groups, specific features). and also describe the steps involved in the synthesis and the role of each step. And most important!!devote one to each step of the synthesis. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesis
- 1. Draw a reasonable arrow-pushing mechanism for the transformation shown along. 2. Identify nucleophiles and electrophiles 3. Name any type of reactions taking place like E2 or E1 4. Account for any regio- or stereoselectivity-Reactions E1 and E2 with AlcoholsIt develops the following reaction mechanisms and the main and secondary products:Draw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic -propyne with 2 equivalences of br2 - no stick structure please.
- Show stepwise mechanism by pushing arrows (fishhook) and drawing ALL intermediates. Draw a detailed mechanism for the addition of HBr to 3,3-dimethyl-1-butene in the presence of dimethlyperoxide. Show and label all steps including, initiation, propagation, and termination.As per the guidelines, three sub-parts will be answered, please help me with these three parts j, k lloudon 6th edition organic chemistry For each of the following reactions,provide the major product(s) or the necessary reagents to perform the chemical transformations indicated. If no reaction takes place, write NRConsider the following reaction scheme: (i) Identify compounds J and K. (ii) Draw a curved arrow mechanism that accounts for the formation of J [please make sure your mechanism takes into account stereochemical considerations]. please can you show how you decide the stereochemistry