Complete answers with mechanism and products, with picture details.
Complete answers with mechanism and products, with picture details. Determine, based on the identity of the...
Determine, based on the identity of the substrate, nucleophile, and solvent, the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistry. OTS DMF y uns + ⓇCN MeCN 3) M Br + H3C-0-
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including the stereochemistry. (6 points) Br + CN acetone d. ~ + CH,CO2H - Y Y + POCHE UCH DMSO + TOCH.CH DMF b. + B + OCH + CH4OH DMSO – w ! ho + OCHCH , CH,CH,OH DM . Br + CH3OH + CH3CH,OH
1.) Determine the mechanism. (Sn1 or Sn2) 2.) Show step by step reaction mechanism of nucleophilic substitution including transition states 3.) Draw the products, including stereochemistry Br + CN acetone
Show the products based on the curved arrow mechanism shown (It's question #2 in the picture, but if you wanted to answer #3/4 too that'd be awesome!) show mechanism ows 2. Show the products based on the curved arrow mechanism shown. V + OH осна 3. Write a complete SN1 mechanism for the following reaction. Br +CH,OH CH₃CH L "CH₂ 4. Write a complete SN2 mechanism for the following. Show the transition state as well. Also list a good solvent...
Based on nucleophile, substrate, and reaction conditions, state the most likely reaction mechanism (s_n 1 or s_n 2) in each example. Draw the products, including stereochemistry as needed. Predict the product of the following reactions:
3. Determine the mechanism of nucleophilic substitution (SNI or SN2) for each reaction and draw the products. Be aware of stereochemistry. 8 + CN - dletone m et och cun, DE Br + OCH₂ CH₂ DME 4. Draw all constitutional isomers formed during each elimination reaction after determining whether it is E1 or E2. habel it as El or E2. госна. a y "ocha, B b. Tă CH₃OH Br -OH
9.61 & 9.63 please Zaitzev's Rule; Intramolecular versus Intermolecular Reactions 9.61 (SYN) Suggest how each of the reactions shown here could be carried out, focusing in particular on the identity of the nucleophile and the choice of solvent. Cl OCH3 Cl OCH3 Racemic 9.62 Provide a complete, detailed mechanism for the reaction shown here. 9.63 For each of the following reactions, provide a complete, detailed mechanism and predict the products, including stereochemistry where appropriate. Determine whether the reaction will yield...
"Complete the reactions showing all Major Products, both substitution and elimination, that can form based on the reaction conditions. Be sure to show stereochemistry where appropriate. Fill in each table with reaction conditions." w upiete the following reactions showing all products, both substitution and elimination, that can form, then circle the MAJOR Foduct(s). Under each reaction, draw the step by step mechanism showing how each porduct is formed. Show or indicate stereochemistry where appropriate. Fill in each table with reaction...
6. Determine the mechanism of nucleophilic substitution for each reaction and indicate the stereochemistry of the products. (in WORDS - DON'T DRAW DRAW PRODUCT BUT NOT Stereochemistry A. Br Brt + CN-acetons B. Br or n + CH₃OH Hochz - + OCHCH DME> c. 7. Label each stereogenic center as Rors A. a c. HO B ...oh OH NH 8. How is each compound related to the first compound D-erythrose (A+B) Oh. HK CH OH 04 I CH -04 D-erythrose...
3. There are two possible substitution products fr products and a complete mechanism for their for IUPAC system and circle the major product. Ustitution products from the reaction of 3,3-dimethyl-2-butanol with aq. HBr. Draw the mechanism for their formation, including all intermediates. Name both products based on the :OH MW: 102. Ts-gimo 4. Based on the reaction above, calculate the theoretical yield for the reaction based on 2.0 g of the 3,3-dimethyl-2- butanol and 5 mL of the 48% HBr....