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- How many stereoisomers of 2-methyl-heptan-4-ol could form? How many would you expect to form? In what ratios? (All equal?). Explain your answer Please explain clearly why the ratio is 1:1. Thank you!On the lines drawn below, provide the systematic (IUPAC) names for the following structures. Be sure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriate. Show some work for full.please provide the machanisms of 1a, 1e, 1f
- On the lines drawn below, provide the systematic (IUPAC) names for the following structures. Be sure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriate. Show work for full credit.How many stereoisomers of 2-methyl-heptan-4-ol could form? How many would you expect to form? In what ratios and why? (All equal?). Explain your answer.Please identify priorities of functional groups and name following molecules based on thier stereochemistry as R or S
- Study the curved arrows in the reactions below and provide the structures of theproduct(s) formed. One block may represent more than one product/by-product.exolain how to solve trial one so i can do the remaining trials on my own. thanksCompound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yne
- Based on the more stable conformation (conformation A), need help providing two mechanisms for the E2 elimination of the protonated version of cis-1 using a general base (B:) to give alkenes 2 and 3. Clearly show which hydrogens meet the stereochemical requirements for E2-elimination Using Zaitsev’s rule, indicate which is favoured. Pictured is also a reaction mechanism to show what the alkenes 2 and 3 are. Thank you :). Write the structure of the product formed in the below reaction and name them. Does the product have a chiral carbon? If yes, assign R and S. Does the product have an internal plane of symmetry? If so, what do you call such molecules? Show the internal plane of symmetry by drawing a line. Please answer fast I give upvoteCan someone explain the answers to 28, 29, and 30? The answers are B, A, A. I understand lindar catalyst makes cis alkenes and Na/NH3 makes trans alkenes but I dont understand how the second step of Br2, OsO4 influences the stereochemistry between the 2 . Will rate quickly if helpful. Thanks!
