C-O-CH.CH. PhầCH, 1. LAIH, 2. water, HCI -OCH CH . LAOR), where tertiary buty Ph-CHE POSTED...
1. LIAIH -OCHCH 2. water, HC CH 1. LIAKOR),H where R tertiary butyl aerny is n. doino y u of uban oCH 2. water, HCl Ph-CH eCH CHO uqo co lo bb . AL 1. DIBAL H O-CHCH Ph-CH 2. water, HC 1. DIBAL H 2. water, HC Ph-CH HO excess H2, metal catalyst Ph-CH excess KOH, water, heat Ph-CH excess KOH, water, heat 1. LiAl 2 water, HC
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...
MOBI (1eq.) 1. Mgº, CH.CH,OCH,CH, 2 Å 3. H,O, HCI 1. CH,MgBr(xs) O 2 H,O, HCI 1. Mg. CH,CH,OCH,CH, 2. 0,0
Canvas Glve the product of the reaction. 1. POL CH.CH OH 2 2 (CH O CH,HCI CH.CH CH O .CH (CH4, ci CH,CHE N Сн, CHE + Сн, но CH.CH CH, H Сн,онун, с CH.CH CH.CH 0 + (он, но CH SAMSUNG CH
predict the products of the following reactions 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0* OCH, NaOCH Ph (2) CH,CH,CH2CH2Br (g) product from part (f) (decarboxylation) 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0*...
Please answer 37-39 Name: ori 1. LiAlH, THE 2.,0 37. 38. CH,CHE-N-CH CH3 + HCI CH.CH H CHE Y E INOCN, DMF, .0 2.LiAlH, ether 39. fultiple Choice Ventify the choice that best completes the statement or answers the question 2 40. Which of the following functional groups does not contain a ca a. carboxylic acid nhuma
7. Show the missing structures in this reaction sequence: 1) (CH),Culi 2) H30* OCH; 1) LAIH CisH2,0, 2) H30* CsH3,02 1) Na, NH (0|2) Hạo* ΕιΟΗ C4H80 00 cushione H2 CH,COCCH Pt D C6H2O3 C C14H3402 C6H2303 HCNICN) 1) KOH HO POCI3, pyridine (causes elimination of water) C, H29NO; C-H.NO, 2) H30 CisH2,0 CrO; H2SO4 HO K.CO, СОСН, — CisH2/03 CH,OSOCH CICH.03 Juvabione, an insect hormone mimic
SO 5. Complete the following reaction HC- CICH 2. CH CH.CH B. HC-6-C=CH- H2O, HgSO Hy Lindlar - C C - CH - Pd 1. BH, 2. H,02 KCN H,0 8. HC-0-2-=CH2 1. BH; HC-C-CECH i. 2. H,02 KOH, Alc., Heat BONAIRE
ta 2.0 L. O .O. HC-CC- 24 d. HC OH 1 2 CH,CHỊU. 2.H,0 c. CH CH 1. SOCH OH 2. LIAHOT-Bus CH,CHE 1. SOCI OH 2 CH CHO Php C ake h. CH CH, NaBH CH,CH, OH 1. AH,THE 2 HOHO I CHOCHEM 1. CH CH CH.CH 3. SO.
1. Write in the product 1. 03 1-sec-buty!cyclopentene > … 2. Zn, H O 2. a) Name this compound according to the IUPAC system: CH,-CH-CHCEC-CH.C(CHa CH b) Write in the product of the compound in 2 a) with the following reagents. Include stereochemistry where relevant. excess H2, Pd/C Na, NH H2, Lindlar catalyst 1) 2) 3) 3. Write in the product of 4-methyl-1-pentyne with the following reagents 1) 2) 2 HBr 3) 4. Show how to transform the compound on...