Please give the major product of any of the given letter a, b, c or d. Explain the mechanism 1)following reactions.Give the major organic product or missing starting material for thea)1. add slowly+ NaOCH2CH32. HCIb)1. NaOCH3, CH3OH2. (CH3)2CHCH2CH2Br3. H3O+, heatōd)2)(NA).1. NaOCH2CH3, CH3CH2OH2. PhCH2CH2Br3. H₂O+, heat1. NaOCH 3, CH3OH2. ?HO3. H3O+, heatClassify each of the following as either aromatic (A) or nonaromatic

1) a)In the given Image, the overall reaction represents the Williamson ether synthesis, where an…

Answered: 1) following reactions. Give the major…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 11E

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Choose the correct reactants for the following multistep reaction: ? O O 1) 1. Hg(OAc)2, 2, NaBH4 2) 1. PCC O 1) 1. LIAIH4 /ether 2. Acid 2) KMnO4 O 1) 1. Hg(OAc)2, 2, NaBH4 2) 1. KMnO4 O 1) 1. HCI/ether 2) 1. PCC 1) 1. HCI/ether 2) 1. H202 CI
To preview image click here. Choose the correct reagent(s) for the following reaction. O A. 1.H20/Hg(OAC)2 2. NaBH4 O B. H20/H2SO4 (cat.) O C. 1. BH3.THF 2. NaOH/H202 OH
Complete the following reaction scheme. 1. DIBALH 2. H3O+ TMSCI Pyridine 1. LIAIH(t-BuO)3 SOCI2 2. H3O+ CrO3 H3O+
Draw the major product of this reaction. Ignore inorganic byproducts. 1. NaNO2, H₂SO 2. H₂O, Cu₂O, CU(NO3)2 Select to Draw NH₂
4. Show the detailed mechanisms of the following conversions. A) 1. Ph,NH 2. H*
Please pronde ne approprate reagents or product. 1.Os0y,TBHP, H20/THF -> 2. TSOH, acetone, PhH,neat 3. AICI3, CH3COCI, CH2C12 2) 1. B200B2,NBS, CC14> 2. Mg, THF;then Pa°Ln, PhBr 3. HNO3 , HzSo4 4. 2n, HCI me Br Me0 (3 meo MeN HN Meo me Br
In each reaction box, place the best reagent and conditions from the list.
5. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. b. C. Ph + PPh3 Cl mylom Ph. CH3 steps steps steps H3C. H3C Ph CH3 CH3 Ph OH ÕH Ph (racemic) 4
Please help…
2. Selectivity. Show the product(s) obtained or the appropriate reagent(s) to be used for the following transformations. a. H Hill 1. CH2N2, Et2O 2. Ac₂O, pyridine A HO₂C ŎCH3 OH 3. cat. OsO4 NalO4 (excess) H2O, MeOH 4. CH2N2, Et2O 1. SAE, (-)-DIPT b. Me 앤 OH 2. MeOH, CSA 50 °C 3a. O3, MeOH CH2Cl2, -70 °C 3b. Me2S B 56%
Question 5 Choose the series of reagents that will convert the starting material to the product. 1. Br2/Light 2. NaCN 3. CH3M9BR 3. H30* 1. Br2/CH3CO2H 2. Mg 3. CH3CHO, then H30* 4. PCC 1. Br2/Light 2. NaCN 3. HOCH2CH2OH/H* 4. CH3CHO, then H30* 1. Br2/CH3CO2H 2. HOCH2CH2OH/H* 3. NaCN 4. CH3MgBr, then H30*
will vote thumb up for the correct answer! plIdentify the best reagents to complete the following reaction.

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