organic chemistry 1.1 pt) Which reagent would you use to effect the following transformation of a...
Give the step by step reactions for the following transformation. You may use the reagents given in the box below and/or any other reagent of your choice during the transformation. Thank you! Multi-step synthesis problem: Give step by step reactions for the following transformation. You may use the reagent given in the box below and/or any other reagents of your choice during the transformation. CООн CI NO2 HBr NANH2 /HBr Br conc. H2SO/conc. HNO3 Cl2/FeCls OHPO PCC HCOOH/FeCl3 CH&Br CI...
I am checking my work conern hydrate reactions and using a new method we learn on synthesis. I need help with all of these questions. Organic Chemistry 2 Which of the following compounds has the largest % of hydrate when warmed in acidic water solution (H3O+) for 2 hours? CCH3 CH CH CH NO2 2.Acetals are often prepared during synthetic sequence to "protect the carbonyl group of an aldehyde or ketone. Such an acetal is NOT reactive to each of...
10% Multi Step Reactions 6) Show how you would accomplish the following synthesis in good yields. You may use any reagents that you wish. Hint: Protect 2 different functional groups if you choose to use a Grignard's reagent. :OH : OH но 10% Multi Step Reactions 6) Show how you would accomplish the following synthesis in good yields. You may use any reagents that you wish. Hint: Protect 2 different functional groups if you choose to use a Grignard's reagent....
Specify the reagent you would use in each step of the following synthesis: 1 pts 2rec step 1step 2 1 pts 2req Reagents Available a. LiAIH4 b. H2SO c. HCI d. HBr e. SOCI2 f pts 2rec f. PBr3 k. CH3CH2MgBr g. pyridinium chlorochromate (PCC) h. NaH i. NaOH .CHyMgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO 1 pts M 1 pts 2req Write the letters of the reagents in the boxes below Reagent for step 1 Reagent for step 2...
D Question 11 6 pts Which structure is a major organic product of the multi-step reaction shown? Recall that the numbers in front of the reagents tells the order of the addition 1) NaNHANH, 2) CH CH Br 3) HgSO4/H2SO4/H,0 // D Question 14 6 pts Which group is considered a deactivator in electrophilic aromatic substitution (EA.S.) reactions? The dashed line indicates where the group is attached to benzene. OH —ОН
2. Reactions: (27 pts) Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'. Ha, Pd/C Cl2, hv A) Br CH, OH B) CH3CH,CH, OH H2SO4 D) NaBH "H CH,CH, OH SOCI TEA OTS E) CH SNa DMSO...
2. Reactions: (27 pts) Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'. Ha, Pd/C Cl2, hv A) Br CH, OH B) CH3CH,CH, OH H2SO4 D) NaBH "H CH,CH, OH SOCI TEA OTS E) CH SNa DMSO...
Specify the reagent you would use in each step of the following synthesis: Cl step 1 step 2 Reagents Available a. LiAIH4 f. PBr3 k. CH3CH2MgBr I C6H5MgBr g. pyridinium c. HCI d. HBr e. soci2 chlorochromate (PCC) h. NaH i. NaOH j. CH3MgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 CHCH3 Reagents Available a. LiAlH4 b. H2SO4 f. PBrz 9. pyridinium chlorochromate (PCC) h. Nah c. HCI K. CH3CH2MgBr I. CHgMgBr (phenylmagnesium bromide) m. (CH3)2CHMOBI n. Cro3 d. HB i. NaOH e. SOCI j. CH3 MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 A(C4H100) reacts with phosphorus tribromide to give B(C4H,Br). B...