2. Fill in the blanks (A-F) for each compound or reagent that is missing in the following synthesis. [Intermediates...

Question

Question

Answer 1

Answer #1

DET NADE Ери Eto- •COOER Neum. u Nch), Naoft cu, I Cricu) 2 Qa W enan Michael addition 430+ Aldol Nao Et Erol

Answer 2

Similar Homework Help Questions

17. Fill in the missing information. Et NaOE H20 ΕΙΟ" EtOH Heat 1. LDA, THE 2....

17. Fill in the missing information. Et NaOE H20 ΕΙΟ" EtOH Heat 1. LDA, THE 2. CHAI NH(CH)2, H* bis 2.H20 NaOEt, EtOH
17. Fill in the missing information. OEt NaOEI H,O EIO EtOH Heat 1. LDA, THF 2....

17. Fill in the missing information. OEt NaOEI H,O EIO EtOH Heat 1. LDA, THF 2. CHI NH(CH4)2, H+ & li 2.H:07 NaOEt, EtOH
Fill in the missing information. OEI NOE EIO H,0 ELOH Heat 1. LDA, THE 2.CH,! NH(CH),...

Fill in the missing information. OEI NOE EIO H,0 ELOH Heat 1. LDA, THE 2.CH,! NH(CH), H 1. 2. H,07 NaOEt, EtOH ** Know how to do all Review of Reaction reactions. (Reagents, reactant categories, product categories). **

Provide a feasible multi-step synthesis for the following compound. Each blank corresponds to a one letter...

Provide a feasible multi-step synthesis for the following compound. Each blank corresponds to a one letter answer. Assume you have enough of your reagent to do the reaction: if you need two equivalence you don't need to repeat the letter. Assume a mild acid aqueous workup at the very end of the reaction sequence. COMPOUND: Starting material and Reagent Bank: D G ce * Br NaOEt, EtOH OEt B E H Br H307, heat Eto OEt F - Br CO2...
4. Guided synthesis. Fill in each of the boxes provided with the missing reagent(s) or product(s)....

4. Guided synthesis. Fill in each of the boxes provided with the missing reagent(s) or product(s). SOC12 | 1 . 03 م 2. H2O NH2 NH2 5. Devise an efficient synthesis for the following transformation (final product is on the left, starting material is toluene on the right). ولكم
2. Synthesis: Fill in the missing products in the synthesis process below. Stereochemistry should be shown...

2. Synthesis: Fill in the missing products in the synthesis process below. Stereochemistry should be shown if applicable. Br m-CPBA NaOEt DMSO H+ MeOH 1. Predicting Products/reagents: Draw the structure of the reagents or the major organic product(s) of each reaction in the boxes provided. Stereochemistry should be shown if applicable. 1) xs LAH, Et20 2) H20 CI HO CI OH CI pyridine

A-C and bottom question In the following starting material(s), reagent(s) or product(s) are missing. Fill in...

A-C and bottom question In the following starting material(s), reagent(s) or product(s) are missing. Fill in the missing material. 1) [H30*), Brz 2) pyridine 1) Bra. PBrg 2) H20 1) Excess NaOH, Excess Bra 2) H30* NaOH Heat о Eto O Heat NaOET OEI 2) H30* DET f.and g. (In your answer include the temperature at which you would you run these reactions?)
2. Outline a synthesis starting from the compound compounds. Fill in the missing reagents and compound...

2. Outline a synthesis starting from the compound compounds. Fill in the missing reagents and compound sis starting from the compound hatow and any other organ ther organic/inorganic PBry COOH
Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or...

Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B, followed by C, and then D, your answer would be: ABCD. NaOH NaOET 1. NaBH4 ext H2O EtOH 2. H20 A B с D E Br H30+ Ph3P=CH2 PCC heat...

missing reagents, please explain 9. (20) For each of the following reactions, fill in the missing...

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