rite the structures for the predicted organic products. In no product is predicted write No RXN. h. i. + [Ag(NH3)2]OH H-2-CH2- H+ OH j. + CH;CO;H O. 2 equivalents
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![Write the structures for the predicted organic products. In no product is predicted write No RXN.
h.
i.
ELOH(xs)
+ [Ag(NH3)2]OH
CH3
H-C-CH2-
H+
OH
j.
+ CH;CO;H
2 equivalents](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F18045e08-fc24-44e1-a1bc-c4700476e725%2F0f857211-d45a-403b-b102-269cbb9dad4e%2Fvr9mjin_processed.png&w=3840&q=75)
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- For the base-catalysed hydrolysis of 3-bromo-3-methylhexane (i.e. reaction with the nucleophile OH-): For the reaction intermediate, draw its structure and give the VSEPR description of the geometry at the reaction centre Give the names and draw the structures of the two reaction products. Explain your conclusions.In the reactions given below, write to which organic molecule Y, Z, T, A ‘belongs, and give information about the reaction types that take place.Can you explain how to predict the major oganic products for this structure? Since there is cirality involved what is the best way to display inversion for this S2N reaction?
- Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the presence of H2SO4 and provide a clear rationale as to why this is the major product of the reaction and the minor product of the reaction.what is the best way to come up with how to synthesize carboxylic acid , oct-4-yne to butanoic acid, or trans cyclodecene to decanedoic acid . I keep getting confused on how to go from the reactants to product, even with the amines. i can't figure out what to use to get to the product. Please explain Grignard rx as well.1. Write in the product of 1-Fluoro-3,7-dimethyl oct-4-yne with these reagents a) ---excess H2,Pd/C----> b) ---Na, NH3------------> c) ---H2, Lindlar catalyst-->
- I’m currently trying to write a lab report for the synthesis of dimolybdenum tetraacetate [Mo2(O2CCH3)4] from the reaction of molybdenum hexacarbonyl, Mo(CO)6 in glacial acetic acid and acetic anhydride under a nitrogen atmosphere, involving the difficult formation of a quadruple bond and requires high heat and long reaction time (approximately 20 hours). But these are the question I’m stumped on: 1. Why need the reaction be done under nitrogen? We also added dichlorobenzene and hexanes during the reaction. 2. Explain the purpose of dichlorobenzene and hexanes. 3. Why does the reaction take 20 hrs?In the scheme below, different products are obtained with the reagents given starting from 2-methyl-3-hydroxypentanal. Write the open structures of the products D E, F, G.A. Without the use of H2 reductions or PCC oxidation fill in the blank steps of the reactions. Final products should be the major organic product.
- Functional groups such as alkynes react the same in complex molecules as they do in simpler structures. The following example of alkyne reaction were taken from syntheses carried out in the research group of E. J. Corey at Harvard University. You can assume that the reactions listed involve only the alkyne, not any of the functional groups present in the molecules. Draw the expected products for the following reaction .Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the presence of H2SO4 and provide a clear rationale as to why this is the major product of the reaction.Consider the following aromatic compounds a para-substituted compound?, the most reactive towards EAS? an ortho-substituted compound? does not react with RX, FeX3?