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- Fill in the missing reagents a-e in the following scheme:What reagents are needed to carry out the shown multi-step synthesis ? Br Br Br Br O 1. 1.) LDA; 2.) HBr 2. 1.) H9SO4; 2.) NaBr none of the shown reagents will work 3. 1.) NaOH; 2.) HBr 4. 1.) Li; 2.) Br2 O 5.6. Multi Step Synthesis. Propose a synthetic route from the reactant to the product using any reagents you need. Nalt LINH4
- 8) What is the major product of the following reaction sequence? 1. HBr 2. NaCN, DMSO3. Propose a possible synthetic pathway for the following reaction. multiple steps20) Draw a stepwise, detailed mechanism for the following reaction. Use curved arrows to show the movement of electrons Br 1) NANH , ( 3 equiv) CH,CH, 2) CH3CH,l Br
- Draw the major product of each step in this reaction sequence. Ignore inorganic byproducts. Select to Draw OH (CH3)3CSI(C H3)2CI, Et3N Bu4NF (TBAF) Select to Draw 1. CH3MgBr 2. H3O+ Select to Draw12) Write the product of each step in the following reaction sequence. 1) НОСН-CH,OH, Н,О* 2) LİAIH4 3) excess MeMgBr LOCH2CH3 4) H3O*Draw the major organic product that results in the following reaction sequence. Br 1. PPh3 2. BuLi 3.
- Select the correct reagents to carry out the following multi-step synthesis. CH3 CH2-Br CH,-OH CHO step 1 step 2 step 3 step 4 step 2 NJOH step 3 PCC CHICI, AICI3 step 4 N8S step 1 n the others.1. Provide the mechanism of the reaction shown in the picture. 2. Explain why it cannot be done in basic conditions. 3. Why is the enol tautomer favored over the keto tautomer? Ph H3C OH H H3O+/H₂O HO H3C Phrank these from least to most reactive in nucleophilic acyl substitution with a nucleophile I)CH3COOC2H5 II) CH3COO-Na+ III)CH3COCl IV) CH3CONH2
