Using retrosynthetic analysis, determine which compound(s) can lead to the molecule shown in a single step. OA OB oc OD OE I A) I B) II C) III D) IV OH E) I or II F) I, II, or IV ?? III IV II
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- The synthesis of an azo dye is shown below. Please answer the following questions. NH2 1) Na2CO3 2) NaNO2, HCI B N-Ñ A Š3H ŠO3 Step 1 Step 2 ŠO3 2 1 1. Why you need to add Na2CO3 in step 1? (multiple answers) Oa)To decrease the solubility of compound 1 - "salting out" ob) To deprotonate compound 1, increase solubility in water Oc) To increase the reaction yield Od)To slow down the reaction rate Oe)To neutralize the HCIIdentify the best conditions to complete the SN2 reaction shown below. N3 A) CHI, THF B) NaCN, DMSO C) NaN», ethylamine D) KI, THF E) NaN, DMFProvide the missing reagent indicated by "???" CI ??? OH (+ other products)
- 1. Predict the products of the following reactions. OTBDMS 1) HBr 2a) Mgo, ether b) c) H3O+ 3) DM Periodinane 4) TBAF 1a) NaNH2 b) c) H3O+ 2) H2, Pd/C 3) NaOCI, AcOHHow many acid-base steps occur in this mechanism? :OH fö OH ₂ H CI: -H₂O (C5H12O) (CsH3O*) :CI: :CI:- yox (C5H1*) (C5H₁1CI)Remaining Time: 38 minutes, 15 seconds. * Question Completion Status: 100 110 120 130 14 15 16 1 36 38 39 40 41 42 430 44 45 46 47 48 49 50 37 QUESTION 2 Which of the following reactions proceeds through a carbocation intermediate? OEpoxidation O Oxymercuration/Reduction O Hydroboration/Oxidation O Acid-catalyzed hydration O Both A and B QUESTION 3 nat alkyl bromide should be used in the acetoacetic ester synthesis of the follow CH;CH;CH;ĊCH3 ve and Submit to save and submit. Click Save All Answers to save all answers. F2 F3 F4 F5 @ # 24 3 W E R
- owing reactions proceeds via an SN1 or SN2 of the reaction: (b) S2 pro85 39 Br tort atubong auonsV HMPAnoitutitaduaHow many different elimination products could be formed in the given molecule? (Hint: include (E) and (Z) isomers) O O A B 3 4 C 5 D 6 Brb) Provide a detailed mechanism (with arrows) and show all relevant reaction intermediates for the following azo coupling reaction. -ZEZ Br NO CIO N Br 'N-