Do problem 19.34 on pg. 741. Phenyl acetaldehyde acetophenone SH CH₃ NaBH. then H30 Tollen's Reagent...
Determine the reagents necessary to carry out each of the following transformations. The reagent choices are listed in the text box above this question (reagents L-U). You will type in one letter choice for each reaction from the list above. No reagent set will be used more than once, but not every reagent set will be used. 7 OH Br 8 OE Br NH2 NH 10 OH 11 Но, 12 NH2 O. Bra L. 1. CH,Br 2. HO M. NaBH...
Give the missing reagent(s). Matching H2SO., H30 Cl2 1) Br, H;O 2) NaH KMnO Cold, Dilute,Basic HCI 1) BH THE 2) H2O2, OH 1) Hg(OAc), H:0 2) NaBH, OH 1) Os 2) (CH3)2S H20, H SO. mCPBA 1) mCPBA 2) H30 Na. 1) OsO. 2) NaHSO; Liquid NH; 1) mCPBA 2) H30, OH Lindlar's Catalyst
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
please help in all sections asap!!!! Which of the following reagent(s) could not be used to carry out the following transformation? HSCH2CH2SH, BFy; then Raney NI (H) 1. NH NH/H"; 2. KOH/H20/heat LAH, ether Zn(Hg), HCI Predict the product for the following reaction. О, Н excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 HO. Η ΝΗΝΗΣ NH2 CH OH CH CH HOCHNHNH OH NH2 NNH2 IN V We were unable to transcribe this imagePredict the product(s) for the following reaction. NaOH...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH d.) o 1. XS LAIH/THF/-78 °C 2. H20 H OH e.) NaNH / lig NH3 f.) Br 1. Mg/THE 2. CO2 3. H30 9.) Ph Ph cyclopropene HF CH h.) OH 1. PCCICH.CH 2. Pri 3. N,Cag) 1. LITHF 2.CO 3. NH.Ca) HNO, NH 1. HNO () 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCH n.) OH XS H.COM acetone OH...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) 30 Unsat. Index = (2C+2-H-X+NY2 = 200 25 e = 2.00 ppm, 4.90 f = 1.27 ppm, 20 720 Compound 18a: C,H,O, singlet, 2H triplet, 3H 127 15 d = 2.66 ppm, a = 7.21 ppm, b = 7.18 ppm, doublet, 2H doublet, 2H C = 4.90...