

1. Draw the products of each of the four steps in the designated boxes (5 points...
please write neatly
1. Draw the products of each of the four steps in the designated boxes (5 points per box). step 1 step 2 PCC H_ H step 3 2) H20, HT step 4 NaOCH3 CH3OH Product
clearer images
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. OH 1. a) Croy, H,SO,,H,O (Jones reagent) b) workup 2. a) HCI (cat.), CH, OH b) workup Q2 1. a) Croy, pyridine, HCl, solvent (PCC) b) workup 2. a) HCI (cat.), CH, OH b) workup a) NaOH, solvent,...
2. Draw, in the provided spaces/ boxes, the major organic products of the following transformations. Be sure to indicate appropriate stereochemistry. If the reaction generates enantiomers, draw one and write tenantiomer' 1. Cl2, H20 2. NaOH На Pd/C 1.Hg(OAc)2 CH,OH 2. NABH 1. CH CO H 2. Hао* Н,с" HC @) 1. ВНа, THF 2. H202, NaOH Br2 CH2CI2 (E)-5-methylhept-3-ene MeOH conc'd H3PO4 ОН Br NAOCH3
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
2. Give the products for the following aldol reactions. (5 points each) 1. Д. ОН: Н 2. н* 3. ОН: Н ОН ".. 5. ОН + CHO 6. ОН 3. Complete the following scheme. Two step reactions will contain two boxes. 5 points MgBr H CI 5 points AICI: 2. H 3. PCC, CH2Cl2 2 points 5 points 2 points 2. H 3. H Cr04 2 points 5 points OH 2 points 1. OH 5 points Final product shows strong...
4.Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction: (20 pts.) H₂ CH₂ CH,OH CH H.C. H₂C Н.С. OCH, CH, 880.
1. Provide the structure of the product (an acetal) in box and a detailed mechanism for the entire transformation (15 points): acetal: inoi Ho Mechanism 2. Provide the starting material AND reagents you would use to synthesize the following product by a Dieckmann condensation. Also draw a detailed mechanism for this transformation (15 points): Mechanism: 3. Provide the products of each step in the boxes provided and draw a detailed mechanism for each transformation (20 points): step 1 step 2...
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 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...
1. predict the major products.
2. draw detailed arrow mechanism.
1. Predict the major product of the reaction. Clearly indicate stercochemistry, if necessary На Lindlarca Me hexanes 2. Provide reagents to achieve the shown multi-step transformations (6 pts)
1) Predict the Products: Using line drawings with proper use of
dashed wedge and solid wedge notation where necessary, draw the
major organic products of the following reactions in the boxes
provided. If no reaction occurs write “no reaction” or “N.R.” in
the box. Include stereochemistry in your answers where appropriate.
If a product is racemic draw both enantiomers or write “racemic”
next to the structure. Assume all reagents written above and below
the arrows are present in excess unless...