please help organic chem sto- cataloa (-) on TEXAS INSTRUMENTS 10. (18) Provide a detailed mechanism...
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11. Provide an electron-pushing mechanism and an energy diagram for the following reaction. Label the energy diagram in such a way that I can tell what structures in your mechanism correspond to what point on the energy curve. You do not need to draw transition state structures, but do label them on the energy diagram as “TS1" ect as needed. (46 points) %. Cat. H+ + H2O HO
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26) Provide a detailed, stepwise synthesis for preparing the molecule on the left below from the molecule on the right and any other reagents necessary Br он
17) Provide a detailed, stepwise mechanism for the base-catalyzed hydration o butanone. 18) Provide the single reagent necessary for the conversion of cyclobutanone to the compound shown below. CHCH 19) Provide the major organ the major organic product of the reaction shown below. CH,C HẠCHÓPhi 20) Provide the major organic product of the following reaction. H2NCH3, H (cat.) 21) Draw a mechanism for the following reaction. no co un C1,0m
Please provide a detailed mechanism
8. What is the major organic product obtained from the following reaction? Но но. он H2SO OH OH 2 3 a. 1 b. 2 с. 3 d. 4 ANSWER: b
Question 10 Provide ALL organic products AND show the detailed, stepwise mechanism for the following reaction. Use curved HE 3 (12pt) INT 11 T Τ Τ Τ Τ Paragraph Arial % DO QO EEE fx Mashups 1 TT, MTML CSS Path: hp
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
please help me with Organic Chemistry/Alkenes problems. Thank you!
Directions: Place your answers to the following questions in the spaces provided. 1. A common problem in the acid-catalyzed hydration of alkenes is the formation of an ether byproduct. Show the formation of the ether byproduct in relation to the reaction below by providing a curved-arrow mechanism for its formation. (2 pts) H30+ Н,0 OH Ans. 2. Which is the correct sequence of steps necessary to complete the following reaction? он...
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Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...
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Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need...