C. A chemist ran the reaction below and got a product. The mass spec of the final product shows that there are no bromine atoms in the final product. What is the final product of this reaction? You don't need to show a mechanism. BrCH2CH2CH2CH2Br + 1 equiv CH3NH2 NaOH ? H₂O
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- ew ons HO. HO. OV от OIV I II D III Select the product of the following reaction. IV H₂O%/ Heat OH HO OH HO П OH НО Ш OHOxidation reactions can be used in multistep syntheses to produce new functionalities for use in subsequent reactions. Consider the following multistep reaction when you draw the structures in Parts 1 and 2 below. Please explain mechanism's fore the products I and 2 но PCC 1. NaH > Product l Product 2 Br CH,C!, 2. Step 1 Step 2 HOChemistry Please also include the mechanism. Make sure to include the major products and any stereochemistry. For each arrow, there are 2 steps involved include those steps.
- please help with all parts of questionSelect the correct product of the following reaction series. 1. NaOEt, EtOH 2. Br EtO NHAC OEt 3. H3O+, 100°C ? H₂N. CO₂H HẠN_CO,H HẠN_CO,H Br I II IIIA chemist carried out a hydrolysis reaction of 1,1-dimethyl-2-bromocyclopentane, shown below. The chemist expected the reaction to yield alcohol Q as product. However, alcohol Q did not inform. Instead a different alcohol was produced. What alcohol? (INFO: the presence of AgNO3 promotes the formation of a carbocation.) Br OH H20 / AGNO 3 Q но OH но он II II IV Select one: A. II В. I С. II D. IV
- Can you identify the reaction and the compound? Reaction scheme ared e. Co Is it drawn correctly? OH M Br ndy: Synthesis the followiong reactions (five only). Pt 1) Cyclohexyne 2H, (850-900)C 2) 3) CH,CH,CCCH, + H;0 2HBR 5) + Zn 6) + HFFor the reaction sequence shown, what is the expected major product? 1. HBr 2. NaOMe ? X X X || ||| IV J