NaN3 HO ΝΗ compound c compound d CI H₂, Pt [References] compound a SOCI₂ SOCI₂ compound d compound e Moclobemide compound b CI The above reaction scheme presents one possible synthesis of the compound. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound e. • Consider E/Z stereochemistry of alkenes. • Do not show stereochemistry in other cases. ▼n [1 ?
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- Give the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal Br a) 2) NaCN, acetone 1) NaOC(CH3)3, heat d Br 2) BH₂ THF; 3) H,O,, NaOH(aq) b) c) d) c) 2) KOC(CH3)3, heat Copyright University of California Merced 2022 Br 1) NaOH, heat 2) MCPBA 1) KOC(CH3)3, heat 2) H3O+CH3man Determine the products for the following reactions (indicate major and minor when appropriate). Show stereochemistry. Josterman CH3 HACH3man . 22 ©2022 an CHE CHCH 22 | Kloster HEM40B W22 ©202 | Klostern NaOEt Br H. Compound#865250 EtOH, Д J Klosterman N22 O Compound#250903 G CompounKlosterrcess o, HEM40B W22 O20 W22 22J Klosterman CH ©2022 J Kloste 2. Zn, ACOH W22 b) rman CHEM4 W22 1. Et,0 armal Compound#903865 CHEM40B W22 C 2. NaOH, H202, Н.о 22| Kosterman 22 I Klos Write your answer in the Answer sheet template.H. H ÔMe Ph;P LIAIH4 compound a compound b HO. Bombykol C16H300 The above reaction scheme presents one possible synthesis of the compound. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound b. Consider E/Z stereochemistry of alkenes. Do not show stereochemistry in other cases.
- What reagents are appropriate to carry out the conversion shown? - OH LOM 1. mCPBA; 2. CH3MgBr; 3. H₂O O 1. CH3MgBr; 2. H₂O O 1. mCPBA; 2. H₂O O mCPBA + enantiomerA eFundi : Home : Overview E NCHE 121 - Module test - Versio X G Which one of the alkenes can for x b My Questions | bartleby + A https://docs.google.com/forms/d/e/1FAlpQLSeaeyD2qYYYa712LcEehfMLha7DEaTq1KXQ5g7o2byUrT8CnA/formResponse Question 4: The alkene 2-methylbut-2-ene reacts with hydrogen cyanide (HCN) to form the Markovnikov product. Write the preferred IUPAC name of the main product of this reaction. [Use lowercase letters. Do not use spaces if it is not required in the name.] * Your answer Question 5: Which statement about electrophilic addition reactions is not true? * Markovnikov's rule explains why the addition reactions of unsymmetrically substituted alkenes are regiospecific. Markovnikov's rule does not apply to internal alkynes. The larger amount of the nucleophile will bond to the more stable carbocation during an electrophilic addition reaction. None of these statements are correct. O All of these statements are correct. Question 6: The mechanism in Figure 6 produces…Arrange the following compounds in the increasing order of reactivity towards Conc.HNO3 & Conc.H2SO4 1. Benzene 2. Chlorobenzene 3. phenol 4. Toluene 5. Nitrobenzene 5,2,1,4,3 5,1,2,4,3 5,1,4,2,3 1,2,3,4,5
- from Ce [Review Topics] [References] Use the References to access important values if needed for this question. Draw the structure of the organic product that is expected when the following compound is treated with concentrated H,SO4. он H2S04 CH3CCH2CH2CH3 heat ČH3 • You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. C P. opy aste C . CH4 ChemDoodle Retry Entire Group 5 more group attempts remaining Submit Answer1. Predict the major product for each. Consider regio and stereochemistry. 1. CPBA 1. MCPBA 2. H*, H20 2. H*, H20 1. Os04 1. ÖSŐ4 2. NaHSO3, H20 2. NaHSO3, H20 1. MCPBA 1. OsO, 2. H*, H20 2. NaHSO3, H20 1. mCРBA 1. OsO4 2. H', Н-О 2. NaHSO3. H20NH₂ NHỊCH, tipy (a) acrylamide Diamines are used as the building blocks for the synthesis of pharmaceuticals and agrochemicals. In the above synthesis, draw the structure of the product (b). ChemDoodle 1. LIAIH 2. H₂O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include cationic counter-ions, e.g., Na* in your answer, but draw them in their own sketcher. OF (b) 6
- Identify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОН2 Use FMO and aromatic transition State theories show that [4+2] -1 [4.2 ] TT S Egcloaddition reactions are forbidden.1. Draw the structure of the major products of the following reactions HO- (1) DMSO, (COCI)2 (2) EtgN H,CrO, H. (1) KMNO,, HO", A OH (2) H,O*