Chemistry Need to write about the green chemistry princliples of the aldol reaction. These are some of the points that should be included. Please help..
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- 10. Explain the reaction shown below. Include the following pieces in your explanation. a. Identify the electrophile and the nucleophile. b. Draw a curved arrow mechanism for this reaction. (Assume an acidic work-up). Explain the electron flow. Indicate any regiochemical or stereochemical preferences. C. d. LIAIH4 OHI. Draw the stoucture of the main product of the following Deactions. Include stereoshemistry, in the product where applisd. 1. HNNH, кон heat. 2. 3. pH S 4. CH,NH, 5. ethanah OH acid. 6. soci, NH,© (7) (8) (9) CHO CHO Br₂ ACOH + HCHO ( con. NaOH OH™ .CI AICI 3 ) ( ) )+ HCOO CH₂MgBr ( (a-halogenation) (Crossed cannizzaro reaction) (Crossed aldol reaction) )
- Match the following schemes to their respective reagents required for the Grignard reactions to proceed. MgBr MgBr MgCl CIMgO + Mg(NH2)CI Choose... OMgBr Choose... Choose... ¶Draw the structure of the major organic product of the reaction. 1. LIAIH4, ether 2. H₂0 ● You do not have to consider stereochemistry. Submit Answer ***I Q CI / Retry Entire Group [ ] در ? ChemDoodleⓇ [F 3 more group attempts remaining view Topics] [References]What advantages and disadvantages of N-formylation? Why do we make it? please 1. abstract 2. introduction 3. methodology 4.result and discuss 5. conclusion
- The following reduction can be carried out with which reagent(s)? Select all that apply O A. Zn(Hg), HCI B. 1) NABH4 (excess); then 2) H20, H* O C. H2NNH2, KOH OD. 1) LIAIH4 (excess); then 2) H20, H* O E. 1) HSCH2CH2SH, H*; then 2) Raney Ni (H2) OF. None of these choicesMethylating agents are substrates that deliver methyl groups to nucleophiles, and so are themselves electrophilic. What is the most common methylating agent (a) in the laboratory and (b) in biological systems? Discuss their similarities and differences... Solve it asapPlease help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)
- help with (Oxidation of Cyclohexanol) post-lab questions. Explain in a paragraph, please. Why does this reaction not work well for tertiary alkyl halides? oxidation of cyclohexanol with hypochloriteUse the reaction given below to answer the following questions. Be sure to include lone pairs (where applicable). A. Br B a) Identify (by name) the frontier orbitals (HOMO and LUMO) of each species. b) Give the name of the functional group in A. c) Draw the orbital(s) comprising the LUMO of A. d) Clearly identify the nucleophile and the electrophile, A or B. : Electrophile Nucleophile e) Draw a detailed, step-by-step mechanism for the reaction given below. Be sure to include all lone pairs and clearly indicate the expected reaction product(s). f) Label each step of the mechanism as either Bronsted-Lowry acid-base, nucleophilic addition, elimination, or other.[Review Topics] [References] Draw the structure(s) of the major organic product(s) of the following reaction. 1. Ithium diisopropylamide /hexane Br 2.1 eq. • You do not have to consider stereochemistry. • Omit products derived from the acidic or basic reagent itself, e g. HN(-Pr)) derived from N(-Pr),. If no reaction occurs, draw the organic starting material. •If substantial starting material is present at the end of the reaction, include it in the products. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with - signs from the drop-down menu P.