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A: Provided dataMelting points:Pure Magnesium: 648°CPure Copper: 1085°CCompounds:Mg2Cu melts at…
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Q: 6. Draw the products of the following reactions. (3.0 pt) NaOH/H2O Η NaOH/H2O дель NaOH/H20 Δ
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Q: 13. Use the half reaction basic solution method. CN(aq) + MnO¯(aq) → CNO˜¯(aq)+ MnO2(aq)
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- (R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed. 2-methylbutan-1-ol 2-methylbutan-2-ol 3-methylbut-1-ene (R)-3-methyl-2-butanol 2-methylbut-2-ene O (S)-2-bromo-3-methylbutaneDetermine the reagents required for the following syntheses. More than one reaction is likely required. a) b) c) d) OH OH olm NH₂ MeO NHMe Me. Me OH OHDraw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexene
- What is the organic molecule X of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.Give the major organic product of the following reaction. 1) ВНз 2) H202, NaOH HO- OH HO There is no reaction under these conditions or the correct product is not listed here.
- A) what is the major product formed (A-D) b) name the mechanism by which the major product is formed c)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.6) Give the products of each of the following reactions. a) b) d) H Li, NH3 CH3CH₂OH xo Na₂Cr₂O7 H₂O, H₂SO4, A H₂O LI, NH3 CH₂CH₂OH
- What is the major organic product obtained from the following reaction? H HC A) 1 B) 2 HO H₂SO4 C) 3 OH 2 سل، ز. مل D) 4 OH4. Aldehydes and ketones can be “protected" as acetals and ketals. Complete the following outlined reactions, showing how the protection is accomplished, and what results after deprotection. MgCI 1) 2) HO* deprotection here2. What is the product of the following reaction? کہا NaOH, H₂O A