12 With only Benzoic acid and Methylamine (CH3NH2), show the stepwise synthesis of Benzylmethylamine. Give the conditions and major organic product after each step. COOH CHINHCH3
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- Devise a synthesis of the ketone hexan-3-one, CH3CH2COCH2CH2CH3, from CH3CH2Br as the only organic starting material; that is, all the carbon atoms in hexan-3-one must come from CH3CH2Br. You may use any other neededreagents.Provide reagents/conditions to accomplish the following syntheses. Several steps are required in some cases. H2N NH2 Но TH. NH2 HOShow and explain reagents and expiramental conditions to synthesize each compound from 1- propanol.
- Provide reagents/conditions to accomplish the following syntheses. More than one step is required in some cases.Give the major organic product of the following reaction. 1) ВН3/THF 2) NaOH, H2O2 HO OH HO- OH There is no reaction under these conditions or the correct product is not listed here.H₂C CH3 Show how the compound can be synthesized from benzene and alkyl chlorides.
- Provide all needed reagents and conditions for each step.Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys fir and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.Provide the necessary reagents to accomplish the desired organic reactions. Please number the steps and note that some reactions will require more than one step. Me Meo. Meo. CF MeO
- Provide the necessary reagents to accomplish the desired organic reactions NH HN HO.Propose single-step and multistep syntheses of acid derivatives from compoundscontaining other functional groups. Propose multistep syntheses using acid derivatives as starting materials and intermediates.A synthetic organic molecule, G, which contains both aldehyde and ether functional groups, is subjected to a series of reactions in a multi-step synthesis pathway. In the first step, G undergoes a Wittig reaction, leading to the formation of an alkene, H. Subsequently, H is treated with an ozone (O3) reagent followed by a reducing agent in an ozonolysis reaction, resulting in the formation of two different products, I and J. Considering the functional groups present in G and the nature of the reactions involved, what are the most probable structures or functional groups present in products I and J? A. I contains a carboxylic acid group, and J contains an aldehyde group. B. I contains a ketone group, and J contains an alcohol group. C. I and J both contain aldehyde groups. D. I contains an ester group, and J contains a ketone group. Don't use chat gpt.