5. Synthesis Design a synthesis of the following transformation. Show how the following multi-step chemical transformation can take place. Provide reagents for each step in the synthesis. Include structures of intermediate products. Do not provide a mechanism or curved arrows. Be neat and clear! Note any special instructions. Clearly label each step in the transformation.. OH

. Devise a synthesis of each product from the given starting material, using any necessary organic or inorganic reagents. Write your answer in the blank space .d) tert-butyl chloride from 1-iodo-2-methylpropanee) 2-bromocyclohexanol from chlorocyclohexanef) trans-1,2-dibromocyclopentane from cyclopentan

Kinetic control At low temperatures, molecules have low amounts of kinetic energy and therefore predominantly react through the pathway that has the lowest energy of activation and therefore proceeds at a faster rate. The product obtained through this pathway is referred to as the kinetic product. ▼ Part B Give the structure of compound A, the major product when the reaction is conducted at low temperatures. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. ► View Available Hint(s) Love + H-Br -55 °C A NN [1] A ⒸH: 120 EXP. CONT Marvin JS by ChemAxon SOZ O IL H N CI Br 1 P F

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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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