option 3
The best way to synthesize the following amine is: HN 1. SOCI 2. ex NH; HO...
Question 32 (4 points) The best way to synthesize the following amine is: HN 1. ex. NH; 2. LiAlH4 3. HO HO 1. NaCN Br 2. LiAlH4 3. H2O 1. SOCl2 2. ex. NH; HO 3. LiAlH4 4.HO 1. NaN3 Br 2. H. Ni
The best way to synthesize the following amine is: HN 1. NBS, hy 2. NaNH, NHÀ 1. HNO3 H2SO4 2. Fe, HCI 3. NaOH 1. Biz, FeBrz 2. NaN; 3. H. Ni 1. NaCN Br 2. LiAlH 3. H20
The best way to synthesize the following amine is: H2N 1. NBS, hv 2. NaNH. NHÀ 1. HNO3 H2SO4 2. Fe, HC1 3. NaOH 1. Br2, FeBrz 2. NaN3 3. H. Ni 1. NaCN Br 2. LiAlH4 3. H2O
What is the major product of the following reaction? NAOH heat X X ger K OH o The best way to synthesize the following amine is: H2N- 1. HNO3 H2SO4 2. Fe, HCI 3. NaOH 1. NaCN Br 2. LiAH, 3. H0 1. Bry. FeBrz 2. NaN 3. H. Ni 1 NBS hr 2 NaNH NHI What is the major product of this reaction! CHU, Hy0°.H20 OH -OH och OH
Question 2 Which of the following is the weakest base? NH, CH,NH HN- H N- - - 0 = 0 = 0 2 0 Question 3 How is N- classified? A a quarternary ammonium ion B a quarternary amine oc a secondary amine OD. a primary amine O E a tertiary amine Question 4 What would be the final organic product of the following reaction? NaCN CH.CH,CI - organic 1) excess LiAlH product 2) H0 . C6H5CH2CH2C02H OB C6H5CH2CH2NH2 CH,CH,CHCN...
Choose the correct starting materials for the following Diels-Alder product: A CHO CHO CHO CHO CHO Doc CHO CHO CHO CHO 2.1 CHO Question 10(4 points) Which one of these compounds is insoluble in water, but soluble in both NaHCO3(aq) and NaOH(aq)? Ophenol O octanal O propanoic acid Op-methylbenzoic acid The best way to synthesize the following amine is: NH 2 H, N 1. NBS, bv 2. NaNH NHI O 1. NACN 2. LAIH 3. H,0 1. H.00 2. ex...
Two pages 30 1) Provide the structure of the major product for ten of the following fifteen reactions. Assume enough reagent to react with all functional groups capable of reaction. NH NaBH,CN 1) MEB 2)H,0 HO NH NaN, 1) NaNO,, H.SO. NH, 2) HBF. KOH 1) odo H30 opas 1) LiAIH, 2) H.O OH h) NH H,SO H.0, A CN 1 cui Oculi O .-780 Br SOCI, NH 1) CHI (xs) 2) Ag,0,H,O, tion N'HSO, H20 Cu_0 Br corond me...
ICA 11-21-2019 (CA Derivatives) Complete the following problems on your own paper. Rewrite the problem 1. Draw the answer to the following reactions, o Nacion 1. NaCN -Br 2 H₂O 1. LAIH 2. H,0 1. Mg 2. CO 4. CH CH CH.CH,OH, H2SO (catalytic amount) 3. HO Br 1. Na2Cr20, H SO4 H20 2. SOCI 3. (CHỊCH,CH, CALI 1. SOCI 2, CH.CH OH 0 OH
1) Provide structures for A-J in the following roadmap. H NaN LiAIH SOCI, CHINH + B с D- CH,OH (xs) CH,OH E+ A CHOS 1) KOH, H20 2) H,07 NH SOCI 2) Propose a mechanism for the following transformation, including arrows to describe electron flow, and all intermediates. CN Oro NaOH H2O are OH
Determine the structures of compounds K-Y in the following reaction sequences. NH MgBr Ho 1. LIAIH4, ether 2. HO 1. NaOH → M- Mchu >N 2. CH CH Br 2. CH,OH ola.ompelen 1. LIAIH., ether PBrs > p 1. PICH) » Q" 2. Bu- H R 2. H2O NaCN OH PBrya 1 V 1. LIAIH, ether 2. 0 .CHMgBrother 2. CH,OH Challe CHET (excess) NaOH, a HGG OCH CHO X- NaOCH,CHY CH.CH OH 2. NHCI