Hi, I need help with this question please!
Hi, I need help with this question please! Week 10 pcrd carbonyl.pl Adobe © © 213...
Hi, Can you help me with this question please!!?? 24 Fischerlwrist 3-23 20.pdf Adobe Acrobat Reader DC iwrkst_3-... * © ☺ 314 o © 75%. I do Below we will consider the mechanisms of the Fischer esterification and acid catalyzed hydrolysis reactions. A typical acid source such as sulfuric acid is used to form the protonated nucleophile. Start here:
23p.pdf - Adobe Acrobat Reader DC Window Help Tools Practice Gradescop... X @ @ Q © © 113 om 1079 - I 1. Given these reactions, answer the following questions: LDA OLI Reaction Which reaction will proceed the fastest? -77 °C LDA Reaction -77 °C Which reaction will proceed the slowest? Reaction 77 °C Which reaction will proceed the fastest? Reaction Type here to search ! @ # $ Practice Gradescopo.pdf - Adobe Acrobat Reader DC e di View Window...
I need help on all of these! Please help with d-h, if possible! d. The reaction of (2R)-butanol with NaBr and sulfuric acid in acetone proceeds with inversion of configuration. e. The addition reaction of HBr to 1-butene in the presence of peroxides produces the anti- Markovnikov product. (Might not be a review question, might make an appearance in early 3060.) The reaction of 2-methyl-2-butanol with HCl produces as a major product an alkyl halide. An ether and an alkene...
Hi I need some help with this synthesis please! The following ether can be converted to the phenol below. Draw a curved arrow mechanism for the reaction sequence.
i need help with this question please 3 attempts left Check my work Click the "draw structure" button to launch the drawing utility Draw the organic product formed in the following reaction. HBr (HyC) CO оснсна CH COOH Енсны draw structure...
Hi! These are some advanced organic chemistry questions and I need help fully answering them. Thank you in advance! Draw a curved arrow mechanism showing all the bond breaking and bond making steps of the following reaction. Draw all intermediates. HINT: begin with a Michael reaction followed by a Claisen condensation. 10 pts 00 NaOET H20+ id. l og Eto V OEt EtOH OEt Draw a curved arrow mechanism showing all the bond breaking and bond making steps of the...
Need help with both 3 and 4 please 3. The reactions below refer to questions 5-7 and illustrate the reaction steps in the anti-Markovnikov addition of HBr to (E)-prop-1-en-1-ylbenzene. Draw curved arrows that account for electron movement in reactions below and classify each reaction according to 6 patterns of radical reactions. reaction pattern Br + Br T + H-Br: - T + :Br. 4. In step a), bromine radical preferentially attaches to carbon C-2 (bromination of C-1 and formation of...
not sure where I was wrong but need help Course Home <Chapter 10 Homework Alcohol Synthesis Using Organometallic Reagents 5 of 19 > Complete the mechanism by adding curved arrows showing electron flow, and draw the products of the reaction of pentanoic chloride with the first equivalent of the given Grignard reagent before it gets a change to react with the second equivalent. Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the grid and...
I only need help with the practice problem using the reactants on number 4. please be specific, thank you. 10/22 be able to predict the products when an alkene reacts with: O MCPBA © Os Oy BH3 | THF followed by HOOH/NaOH H2SO4 H20 ② H₂ Pdlc (be extra careful about drawing products comect stereochemistry) CH3 CH3 Practice try eacting this alkene with the 5 reagants above. Draw the major product for each reachou. CH
hi can someone help me with the mechanisms on this! i need major help! 11.Draw the structure of the major organic product(s) for each of the following reactions. Indicate the stereochemistry for each reaction when it can be determined. In addition, write 'racemic' if a racemic mixture is formed. 3-chloro-3-methylpentane water ethanol alcohol a. SOCI2 pyridine c. Sec-butanol CH=CH2