8 (ppm) 0w 8-72 (a) Simple aminoacetals hydrolyze quickly and casily in dilute acid. Propose a...
Propose mechanisms consistent with the following reactions 8-48 H.SO н.о Br HBr ъ) Он (а) ROOR Br СHBE, Вг Br Вг HЕr (d) NaOH осH CH, Cl Вr НС Br Br CH CH OH Cн CH, Он Н н'. Н,о Он Н "сн CH, CH,CH CH,CH Он н' (g) CH Oн осн, н CH—С-С (h) 2 н Н Н Н Propose mechanisms consistent with the following reactions 8-48 H.SO н.о Br HBr ъ) Он (а) ROOR Br СHBE, Вг Br...
if anyone can check these answers for me and tell me which are right or wrong id appreciate it 0. How can p-aminobenzoic acid (a sunscreen) be synthesized from benzene? (Note that sometimes more than one isomer will be obtained, which is fine as long as the desired isomer is one of the major products.) several steps HOOC 4. Sn, HC 4.KMnO. .KMnO 4.Sn, HC 3.KMnO 3. CHCI, AİCİ, 3. Sn, HC . HNO, H SO 2. HNO,, H:SO4 1,...
7. which pairs of reagents will best provide the alkene shown? 8. 9. 10. 11. what is the form of Aparetic acid at Ph=1? 12. what is not an intermediate in the mechanism of the following reaction? MacBook Air 80 Question 8 (2.5 points) 1. CO2 MgBr 2. Hot ? Next Page MacBook Air Page 8 of 20 80 Question 9 (2.5 points) O(CH2CH2)2Culi CH3CH MgBr O CHỊCH-Li CH,CH,ONa Previous Page 23 Page 9 Submit Quiz 3 of 20 questions...
QUESTION 1 Any reaction involving a carbonyl group and a strong acid begins with the same first step, which is __________________ of the carbonyl oxygen. QUESTION 2 Using condensed molecular formulas (C#H#X#Y#) for your answers, predict the products of the reactions of C6H5CH2CHO (phenylacetaldehyde) with these reagents, and identify the functional group produced in the product. Note that the Tx symbol above allows you to do a subscript. a. NaBH4 / CH3OH b. 1. CH3MgBr; 2. H2O c. Ph3P=CHCH3 d....
can you solve 7 and 8 please? 7. Propose structure(s) for the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry. a. O CH3CCH3 + CH3CH2MgBr 1. ether 2. H30* b. -[O] CrO3 H20 OH C. CH3 + CH3CH2NH2 1º amine 8. Write the complete stepwise mechanism for the Grignard reaction shown below. Show all intermediate structures and all electron flow with arrows. OH C-CH2CH3 1. in ether CH3 CH3CH2MgBr 2. H, H2O O=0...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocyclic amines i Cho OH HOH OH LCH, HOW N & CH₂ IN-CH HO (e) (b) 11. What is the IUPAC har is the IUPAC name of the following compound pound? OOH 9 TOH OH 9 hydroxy-1.4-dimethyl-5-oxohexanoic acid hydroxy-2-methyl-5-oxohexanoic acid (d) 2-hydro ydroxy-2,5-dimethyl-6-oxoheptanoic acid 2-hydroxy-1-methyl-4-oxopentanoic acid (e) 3-hydrox 3-hydroxy-2,5-dimethyl-5-oxohexanoic acid O 3-hydroxy-2,5-dimethy 12. Predict the product/s, the product/s, if any,...
practice questions ③ show the product on products Expected for the reactions below a) + CH₃OH alcohol c-c-c aldehyde c-c-c acid C b) 014 + CH3 CH alcohol ÖH c) -10 kmnog LOH heat (Excess) cox - Bonus! 0: CEN: d) -10- H₂ Pd/c. (Excess H2) (Red) H -Bones! e) ÖH ć. + -10 alcohol он acid croch Grid x + CH₃ CH₂ 0 4 (drohol) -10 NH₂ 3 continued - show prodoct (s) رخ دن 2) 15 PH:10 NaOH...
Please analyze the IR and NMR spectra. How pure it is? What impurities can be observed? Please label all major signals. The product is N,N-diethyl-m-toluamide. The product is obtained by the following reactions Solvent is Et2O. Extracted with NaOH and then HCl and then H2O. Dried and then evaporated. To further purify the product, hexane was added to perform column chromatography. Evaporated. Clearer image for the IR image: CH3 CH3 SOCI2 + SO2 O=0 ОН CH3 CH3 -- + excess...
could you please help me with these questions. thank you so much 20. Which reagent would best serve as the basis for a simple chemical test to distinguish between 0 0 CH3CH2CC2C3 and CH3CH2CH2CCH3 a. NaOI (I in NaOH) b. Br CCL c. CrO,/H SO d. NaHCO,/H20 21. Which proton in the following molecule is the most acidic? A) 1 B) 2 C) 3 D) 4 E) 5 22. What product is formed in the aldol reaction of propanal? a....
practice complely the follow, + NaOH following (Fill in the Blanks (ose wnds carboxylic Acid + Amine water carboxylic Aad & Alcohol Carboxylic Acid water Esten + H₂O + tre hydrolysis? Amide + H₂O titre hydedlysis Show the reagent / reagents needed to make the following molecolar conversions. Show reagent (s) to the right. Seach=40 HC=CH₂ HC-CH₃ 4 ة= SH please note: the is an aromated ring. It does not atlect the chemistry Hocao 0 ÖzçēH (oxidation? bacco in there...