1. Write the mechanism of the following reactions. Also, explain the stereochemistry of the reactions. alt...
write the mechanism of the following reactions 1. Write the mechanism of the following reactions. Also, explain the stereochemistry of the reactions OH SN' H Sur عی
Write the mechanism of the following substitution reaction Explain why Polar protic solvents favor SN1 reactions. Do you expect this substrate to react under SN1. explain your answer.
1. Determine whether the following reactions go through SN or SNP and write the products, with stereochemistry as applicable. BrNHz NaOEt Nal OMS KCN CI DMSO Br HO NaSH DMSO Tso CH3 Nal Acetone CH3 2. The following reactions each undergo SNmechanisms. For each explain why you would predict the substitution products to come from an SN2mechanism and fill in the product. If stereochemistry is given in the reactants, give the correct stereochemistry in the products. Cl + Z Na...
For the following substitution reactions predict the products showing stereochemistry only if is of relevance. Also comment on what type of reaction: Sn1 or Sn2. Finally is the starting material and product optically active or inactive? Explain. CH3CH2CH3 НО HBr CH-Br НЫС
Can someone explain the mechanisms + products for these reactions? 1. (3p) Draw the mechanism and the expected reaction product for the following reaction: ? 2. (3p). Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: ? OH
Write products of the following reactions. Indicate stereochemistry(using wedged and dashed bonds)when asymmetric centers are produced or changed. a. b. c. H SO4 1-hexanol HSO d. 0 pKa of conjugate acid is 5.2 e. Ci Cl OH
ALSO DRAW THE MECHANISM FOR THE CORRECTED 3B 3. The reactions below would not go as planned. Br NaoEt i. Explain why the reaction did not go as planned. ii. What product would form? iii. How would you change the substrate or the reagent to produce the correct product? 1. LIN(IPP) 2.B part + LIBr + HN/IPr)2 i. Explain why the reaction did not go as planned. ii. What product would form? ill. How would you change the substrate or...
Please explain and right in details 145 1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: NaOCH, Br a) H2O2 - b) NaOH 0-s- 4.5 'o:
please do all and explain sn1 sn2 e1e2 1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. CH-Oн heat NaOCHs + HBr HG OH Nal Hо acetone NaBr +HBr 2. Predict which reactions proceeded by an SN1, SN2, El or E2 mechanism: NaOCH CH +NaBr оснCH Носн,сн, 50° +NaCl Nal DMSO, 45 Br NaOCHa +NaBr +HOCH Носн, 100° но +HI acetone, 50 HSO +HO HO,...