Retrosynthesis: Show how one could carry out the following synthetic transformations using any necessary organic and inorganic reagents. Multiple steps may be required in some cases. Label each synthesis with the corresponding letter as you write it.

Synthesise the target molecules drawn below using precursor chemicals within the following limitations: 1) ALL intermediates and reagents must be shown.2) Each molecule requires multiple step synthesis.3) You must also synthesize any organometallic reagents or ligands that you wish to use. a) Aspirin is a common pain killer that was developed by Bayer.

what reagents would it be?

Draw all steps in a proposed synthetic pathway to convert the starting material to the compounds shown below. You can use any inorganic reagent(s), sodium methoxide, sodium tert-butoxide, LDA,n-BuLi,m-CPBA, pyridine, PPh3, DCCand pyrrolidine. These conversions may take more than one step. Include all required reagents (solvents are not required), mechanisms are not required.

Synthesize the following ether from any two alcohols. YOU MUST SHOW the complete retrosynthetic analysis as well as the reagents you would use in the forward direction.

3. ( series of reactions, you could use to synthesize each compound (in the best yield possible) given the organic reactions you know so far. You must use the starting material shown, but may use any inorganic reagent, common solvent, or temperature you need. Don't show mechanisms here. (You are welcome to use scratch paper to work out your ideas, though.) Synthesis. Complete 2 of the 3 syntheses below. Show a reaction, or Make this... From this... Benzene, and any organic compounds needed containing 5 or fewer carbons. a Benzene, and any inorganic compounds needed. .CI Benzene, and any alkene or alcohol needed containing 6 or fewer carbons.

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

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Give detailed Solution with explanation

1 Using this retrosynthesis scheme, Show a forward synthesis with all relevant reagents and conditions needed to make the desired molecule. Don't show mechanism arrows or intermediates.