Can you explain how you came upon the answer also 1. Rank the following compounds in...
2. Predict the MAJOR product(s) for the reaction below. Pay close attention to stereochemistry. Provide a mechanism as to how you arrive with your answer. If your compound is chiral, indicate the configuration [(R) or (S)) of the product(s. H-Cl на. 2. Predict the MAJOR product(s) for the reaction below. Pay close attention to stereochemistry. Provide a mechanism as to how you arrive with your answer. If your compound is chiral, indicate the configuration [(R) or (S)) of the product(s....
Can you please explain how to solve only 7.62 and 7.64? As well as 6.28 a and b. Rank the three carbocations shown in terms of increasing stability: 6.28 (a) nobicnensh (b) owllo or 3 DE 7.62 Predict the stereochemical outcome for each of the following E reactions. In each case, draw only the major product of the reaction (a) ? NaOH (b) CN Br (a) (c) ? NaOH in the substrate. in the product. CI (b) (d) of configuration?...
Rank the following compounds in order of decreasing acidity. Br ОН Br OH CI OH FF SH CI B A FF c D D>C>B>A A>B>CD OCD>A>B C>D>B>A Rank the following compounds from the most stable to the least stable. А B C D D>B>A>C A>C>B>D OC>A>B>D OC>A>D>B A>B>C>D Which one of the following compounds will have the lowest wavenumber for the carbonyl absorption? NH2 IV OIV OV OM What is the major product of the following reaction sequences ? 1)...
thank you!!! 1. Identify the configuration of each chiral center in the following compounds. Draw the enantiomer for each of the following compounds. OH Br b) HO H c) *** 4 Name CHEM 2200-Summer 2020 OH d) OCH e) -OH CI
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable and 4 least stable). н н сH н Н,с Н,с" H сH; CH3 Hас- H 2. (6 pts total; 2 pts each) Complete the following transformations by indicating the reactant structure or the major organic product(s). Place your answer(s) in the space provided. Be certain to indicate stereochemistry where applicable. Cl2 Он cat. H2SO H-о Br Br conc. HBra) сн сна 3. (10 pts...
are these correct? if not, can you explain? thanks! 6. Rank the following, with 1 being highest/most. (2 points each, 16 points) Stability Stability Heat of Hydrogenation Reactivity towards Cl2 addition (No Lewis acid, no hv) d. 2 Br Reactivity towards Sn2 attack by NaOCH, H H - Br I Br Cation Stability. (Remember that other resonance structures also pertain and impact the overall stability of the cations.) Br Насо 3 Reactivity towards reaction with cyclopentadiene Reactivity towards Sn1 substitution...
1. Draw the (major) organic products of the following reactions: HNO3 H2SO4 HN (CH3)3CBr AlBr3 FeBr3 Br Sort the following molecules by their reactivity toward electrophilic aromatic substitution (1-most reactive, 4 2. least reactive): NH2 so,H Place either the letter A or C below the following compounds to indicate whether each of them are achiral (A) or chiral (C) 3. но Cl Determine the configuration (R or S) for each stereocenter in the following compounds: 4. Cl Cl NH2 но...
Can you please draw it and explain Which of the following compounds is the product of the reaction shown that displays retention of configuration compared to the starting material? H2O Sni a . H d. HO, b. Br CH3 H H3C он OH c. CH3
PLEASE HELP WITH THESE. THANK YOU How are the following two compounds related? CH CH3 HO -H HO -Н Given the following substitution reaction, what would the effect be of changing the solvent from CH3OH to (CH3)2S=0? H- OH H OH VS HO -H H -OH H -OH HO H + CH (CH2CH2-Br NaOH CH;(CH2), CH2-OH + NaBr CH OH CH2OH A. The reaction rate will increase. OB. There is no effect on the rate of the reaction, C. The...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...