based on the reactivity of the reagent the products are
as follows
complete the followimg synthesis 121. S2 NazCkOz H2SO4 D ETOH CHI Sou F 1. Li Acoelsh...
121.52 stude Na₂CKO H2SO4 EtoH CHA Souz 1. Li ACORl₃H 2. H2O ں ډ
Complete the products of the following sequence of reactions OH OH EtOH / acetona H2SO4 cat. 1. Meso Cl, piridina 2. KCN en DMSO 1. LIAIH4, THE 2. H307 HO c OH A B
1. Which reagent could be used in a Williamson Synthesis of cyclohexyl methyl ether? H2SO4, NaCl, H2O, or NaH ----------------------- 2. Which carboxylic acid is the most acidic? --------------------- 3. A reaction that would give n-hexyllithium is: CH3CH2CH2CH2CH2Br + 2Li CH3CH2CH2CH2OH + Li CH3CH2CH2CH3 + Li CH3CH2CH2CH2Br + LiBr CH3CH2CH2CH3 = CH3Li ---------------------- 4. Starting with p-bromoanisole, what sequence of reactions will produce p-methylanisole? 1. CH3l 2. Mg, ether 1. Mg, ether 2. CH3l 1. Br2, AlBr3 2. Mg, ether...
2. Fill in the blanks (A-F) for each compound or reagent that is missing in the following synthesis. [Intermediates can be provided if you get stuck - no credit for those provided.] H0+ LOE NaOE Eto EtOH 1. LDA, THE 2. CHI DO NH(CHỊ), H* 2. Hot NaOEt, EtOH
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...
Choose from the following list of reagents: RCO3H H2, Lindlar's cat. 1) Hg(OAC)2, EtOH 2) NaBH4 1) NaNH2 2) MEI Na, NH3 1) H2SO4 2) EtOH 1) NaNH2 2) Eti 1) NaOH 2) Mei 1) RCO3H 1) RCO3H 2) EtOH, [H2SO4] 2) MeOH, [H2SO4] 1) Br2, H2O 2) RCO3H 1) Br2, H20 2) Mei Enter the correct letter for each step of the reaction in the boxes below. (Reagents can be used more than once.) Step A: Step B: Step...
5. Complete the following synthesis and draw the mechanism of step 5. O Na Step 1 Step 2 Step 3 Na2Cr207, H2SO4, H2O Step 5 HCI, H2O Step 4 Mechanism of Step 5:
Need Help. Will Rate If Complete. 1) NaoEt, EtOH Br 2) O 3) H30+ / A. 1) NaoEt, EtOH (s) ar 2) Y Br 3) Hz0+ / A 1) NaOme/MeOH ~ Br OMe 3) Hz0+/A. 1) NaOEt, EtOH 2) V Br 3) NaOEt, EtOH COOEt 5) H30+/A Robinson Annulation NaoEt, EtOH/A come lui OMe 28- The following molecules can be formed by either: Michael Reaction; Enamine Acylation; Acetoacetic Ester Synthesis; Michael Addition; Malonic Ester Synthesis; Robinson Annulation; Aldol Condensation; Claisen...
QUESTION 18 What reagents can be used in this synthesis: OH OA. 1) LiAlH4. 2) H2SO4. 3) DCC. OB. 1) Li. 2) methyl acetate. 3) HCI. OC. 1) DIBAL. 2) 2-propanone. 3) NaOH. OD. 1) Li. 2) acetyl chloride. 3) KMnO4- O E. 1) Mg. 2) acetone. 3) H2S04.
Complete the following synthesis by selecting from the list of 14 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 and then C, and then D, your answer would be: ABCD. OLU SO3 Br2 PBra OH H2PO2 1. LiAlH4 2. H20 NaNO2 HCI H2SO4 FeBrz H2O, heat HNO3 NaBH3CN NBS...