Organic Chemistry
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Organic Chemistry **please explain step by step **please answer both Questions and ALL parts!! 1) Rank...
Organic Chemistry **please explain step by step **please answer the Question and ALL parts!! 7) Predict the product of each of the following reactions. MgBr, Et20 i) H30+ O. a) ii) Etl b) H30+ c) i) Et2CuLi li) H3O+ d) HO Ag20, THF, H2O e)
Organic Chemistry question partial step of a synthesis. Can someone explain the mechanism? Thank you. c) NaOH, H2O O O HCI, H20 d) Heat cyclobutyl methyl ketone
could you please help me with these questions. thank you so much 45. What is the order of decreasing reactivity of aldehydes, esters and ketones? a. Aldehydes > esters >ketones b. Esters> aldehydes > ketones c. Ketones > esters > aldehydes d. Aldehydes > ketones> esters 46. Which of these will not catalyze the reaction of a weak nucleophile with the carbonyl group of an aldehyde or ketone? (Hint: Look for which is not a Lewis Acid) A) I' B)...
Organic chemistry reaction 1) Ethers 2) Organometallic compounds Please explain, thanks! Ethers tr Decide Snul or SN2 A Complete the reach on H -I SN2. H-I (2 organometallic compounds Br Mg duhhyle her 2, H20
please give correct answer to these 5 questions with explanations if possible, thankyou During a nucleophilic addition reaction between LiAlHe and a carbonyl compound, what atom is the nucleophile? Select one The proton (H) atom The hydrogen atom of the lithium aluminium hydride. The aluminium atom. The carbon atom of the carbonyl group. The oxygen atom of the carbonyl group Why do carbonyl compounds undergo nucleophilic addition reactions ? Select one: The compound the carbonyl group is reacting with is...
Please answer both parts h Provide the produet and a detailed step-by-step mechanism for the reaction below 20 points) Na OCH, in CH OH 5. (a) Enamines react with acid chlorides in the same way as do other nucleophiles, and the result (after workup with water) is a dicarbonyl compound; this is sometimes called the Stork enamine acylation, after Prof. Gilbert Stork who developed this chemistry. No new ring is formed during this reaction. Please provide the product and a...
Organic Chemistry **please explain step by step **please answer the Question and ALL parts!! Experiment #5: Multistep Synthesis Part C: Preparation of 5-(2-(diethylamino)-5-oxocyclopent-3-en-1-yl)-2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-olate. ----->. (Compound 5) Question: Interpret the carbon-13 NMR spectrum. INDEX FREQUENCY PPM HEIONT le Nane: 26173.อ 19493.5 17347.7 138.040 5.3 13037.1 103.73 21 208 ,265 155.114 Data Collected ont 46.7 Archive directory: honewalkup/vnnrsys/data Sampie directory 9119.472,565 13.2 JRAC_20150429 01 8379.4 66.67 46.5 544.i 44.11659. 3083.6 24.537 36.8 1167.7 Fidf ler pslab 1.02 Pulse Sequence: CARBON (2pu1) Solventi...
Please explain the reasoning behind the answer. (A) Which of the following molecules behaves as both an X- and L-type ligand to a transition metal cation CH3 CEN H3C CH3 (C) Which organic halide shows the largest reactivity towards nucleophilic substitution by ethanol? H Br Br H Br H Br
Please help organic chemistry provide a reasonable reaction mechanism for the following reaction Answer both parts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic regents provide a mechanism for each step of the following process.
organic chemistry A carbonyl group, C=O, and an alkene, C=C, double bonds, are both sp2 hybridized. However, the chemistry of these two functional groups is very different. This can be explained by which of the following statements? a. The bond angle of the carbonyl is larger than the bond angle of the alkene. b. The electronegative oxygen of the C=O group makes this bond polar. d. There is more steric crowding in the carbonyl than in the alkene. Which, if...