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please write clear ☺️ thank u!!! to fill in thr reagents necessary to get thosr products...
fill in the blank. for thise blanks that corrwspond to products fill in the major product. for blanks corresponding to starting material or reagents fill in the appropiate compounds to give the product in the highest yield Organic Chemistry 1-Worksheet 11 Br, NaOH Cl, HOAc Orga , NaOH Orga он CH,N CH,CH,OCH,CH CH2Cl, 30 min "ОН
fill in the reagents to get the given products CI ?? i. CI H Br Br. ?? ii. ?? Br он iii. ?? но iv. OPr ?? V. ?? vi. Он ?? vii. OTs ?? н. Н. N viii. ОН ?? ix. Cl AL H-
answer all questions 5. Fill in the missing structures (products or reagents, including stereochemistry, if relevant) and specify the most likely mechanism (SN1, S2, E1, E2) for formation of the product you have drawn. If a mixture will occur,show the major products. CH,ONa Сн,он нсулснэ H₃C Br HO H2O/acetone H₃C LIOH CH₂ H₂c a DMF 6. For the series shown below, label the most stable alkene, and the least stable alkene. CHE CH, CHE CH, -CH3
Please explain!! Thank you!! I will rate! Fill in either the missing product or reagents (over the arrow) CH H3C CH2 KmN04 H2C1 CH3 Lindlars H2C OH H3c
Please Print! 2. Fill in the missing reactants, reagents & conditions, or products. Show stereochemistry where appropriate. 10 points. MgBr OH then H30+ „CH₃ HAN CH3 Ht cat MgBr N-CH₃ Мео (then H30t Meo он NaCN -CH3 CH₃ OTS CN or CH "CH₃ +
please provide me with the detailed right answers with clear hand writing please thank you so much. [1] Draw the chemical structure of the reagents and products to prepare compound (A) starting from Benzene. This is a multistep preparation. COOH O- - - SOZH Compound (A) [2] Identify the absolute configuration of the chiral carbon atom (with an asterisk) if it is [R] or (S). Show the priorities and rotation. (The atomic numbers are H=1, C=6, N=7, O=8, CI=17] HO...
missing reagents, please explain 9. (20) For each of the following reactions, fill in the missing reagents for the formation of the product shown. Sequential steps. numbered. Reagent List: reagents from the list provided s necessary, should be HyC-Br Nah NaOH H,C- CH ( MCI) HBECH,OH Br-Br O=C=0 HOÀc) (LDA) 041 H2o depromat ΝΛΗ noad to Nattpostele Br Br-Brz H3C H-BK H4C1-NH2 H3C H,C CH, Br H2C+NCHE HEC CH2 LOA B
II. Reactions: Predict the major organic product(s) or write the appropriate reagents/starting materials for the following reactions. Indicate stereochemistry and regiochemistry when appropriate. Indicate reactions that are expected to result in a racemic mixture of products DBr 1. Н.О, CHCI он HSO, heat кон 1) вн, THF 3. 2) H202. HO 1) Hg(OAc)2, CH,OH 2) NaBH, OH 5. Br2 SH 6. HIO4 OH THF, H2O "он III. Synthesis: Starting from the alkenyl bromide below, devise a synthesis that produces the...
3. Fill in the reagents or products for the following reactions. Note some boxes will require two or three reagents in separate steps; list them as 1, 2, and 3. (2 points) 1. MeONa/MeOH 2. HCI +/ H2N Br 4. Using another sheet of paper, provide a reasonable reaction mechanism for the following transformation, starting with enamine generation (Carbonyls 2) and subsequent alkylation and hydrolysis (Carbonyls 3). Please write neatly and show all arrows, resonance structures, tetrahedral intermediates, and charges....
please solve clear with number , thankyou ????? 5. [14 pts) Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below showing whether it is a Syn or Anti addition when applicable. No mechanism required! (3 points cach organic product and 2 points for the stereochemistry. Adding the stereochemistry when it is not needed will be penalized) A HO Acidic...