please explain each step of this reaction
(organic chem)
please explain each step of this reaction (organic chem) H2N NH2 Hасо. Hао" H* осн, -...
Н,о" CH3 H ОН ОН Но HCI Hасо оснз НСI CH,он TSOH CH,сH,он осн TSOH Он CH,он Hао" о о-
please help, if you can NHCH AICI ? For the reaction above, which of the following is/are the best choice(s) for the final step of the mechanism? NHCH3 NHCH3 A anács Cl--AICI, AICI + NHCH3 AICI: + H- AICI NHCH mo NHCH D C + AICI c- Aici E both A and D F none of the above + Bra FeBry For the reaction above, which of the following is/are the major organic product(s)? O OCH o= OCH 0 E...
please help me in all sections asap!! Predict the product of the following reaction sequence. NaCN 1. LiAIHA HCN 2. H2O H2N NH2 но NH2 но но CN H2N H2N IV We were unable to transcribe this imagePredict the product for the following reaction. ОН excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 CH H_NHNH2 NH OH 0 CH CH NNH OH HO NHNH 0 NH IV v Predict the product of the following reaction sequence. NaCN HCN NH2 H2N но...
Determine the product for each reaction. HBr А. CHa он Br ОСн-CHз "он он осн-сHа mCHA [11 CH3CH2O Na В. ОН -С—С—Н T I CH3 H Нас [2] H20 OCH2CH3 TE OH CH3 "Вг Н-с-С—CH он A OCH2CH3 CH,CH-он С. Нин. nCH3 "CHз H2SO4 H
1. Predict the product(s) for each of the following reactions: H2SO4 NH2 a. 0 1. H2N-NH2, H2S04, -H20 H 2. KOH/H2O b. MeOH, TsOH он H2O C. H2SO4, -H20 HO d. H2O, H30+ e. H20,H30+ 2. Predict the product and draw the full pushing arrow mechanism for the following reaction NH2 H20,H30+ a. b. 3. Devise an efficient synthesis for the following transformation. HO Br Br
Give the product(s) of reaction of hexanal with each of the following reagents. 2. (0) носн,сн,он, н (b) 1. LIAIH, 2. H,0* (e) NH,он, н" (d) NH,NH2, KOH, heat (e) (CH),СHCH,CH— P(C, Нә» , н" (g) Ag, NH, H,O (h) CrOs, H,SO H,0 () 1. KCN, 2. H,SO MCPBA Give the product(s) of reaction of hexanal with each of the following reagents. 2. (0) носн,сн,он, н (b) 1. LIAIH, 2. H,0* (e) NH,он, н" (d) NH,NH2, KOH, heat (e) (CH),СHCH,CH—...
please explain your answers PROBLEM 6-26 Propose a mechanism involving a hydride shift or an alkyl shift for each solvolysis reaction. Explain how each rearrangement forms a more stable intermediate. сH, ОСН, -CH-CH, + Cн, —С—СН—СH, CH I (a) CH,ОН CH, C- CH,—С—СН— СH, heat HOCH, CH CH3 biod Iyinsgoon OCH,CH CI CH,CH,OH (b) + llt noi obimt OCH,CH, bouCH heat CH CH3
Predict the product by providing the stable organic products for each reaction. NaBH4, CH3OH 1. н 2. HСI, Н20 н Н NaBHa (0.50 eq.), сH,он 1 2. HСI, Н20 LIAIH4 (1 eq.), THF 1 2. HC, H,о NaBH(ОCH;)з. (1 еq.), CH,он 1. CI 2. HCI, Н20 о
organic chem 2 pllease help 1. Complete the following: (2 pts each) 10 OCHO + PCHACHO OH (6) CH-cp+ o co Chs 2 hot 1) CHO O Ol (c) HCHO + CH₃-CH O OH (d) Chica Complete the reaction and provide a stepwise mechanism: CH3 OH (3 pts) Он- (b) (4 pts)
(24 pts) 3. Predict the product(s) for each reaction. Indicate stereochemistry if known. If more than one product is predicted, circle the one you think would be major. If there is no reaction expected, then indicate NR. а. HaCl.. Br NaCN THF b. Н—Br ether ОН с. CH3 КОН Br THF d. НОСН heat е. PBr3 ОН ether f. ОН NaSCH3 Hо g. cat Br H2SO4 heat ОН h Br H но heat Br