fill in the reagents to get the given products CI ?? i. CI H Br Br....
(Matching) Complete the following reaction by selecting the most appropriate reagent or reagents for each missing step. 1.227 2. CH,Br 3.222 OH EIO 4.272 5.772 NaH H30* heat soch III NaBH, ETOH ETOH NAOH THE CH,CH,Br V VII VIII IX х CH,Be Br Br CI XI XII XIII XIV XV XI XII XII XIV 1st Step 3rd Step Choose ) V VIII XII X IV II IX XV XIII VI XIV XI III VII 4th Step - 5th Step <...
What compound is likely to be obtained via the following reaction sequence? i.HONO, 0-5°C NH, Br Br ii. CuCl iii. Fe HC1 NO2 i. NaOH. H,O v. HONO. 0-5°C vi. HyPO2 CI Br Br Br Br Cl Br Br Br Br Br Br NO2 Cl IV
What compound is likely to be obtained via the following reaction sequence? i.HONO, 0-5°C NH, Br Br ii. CuCl iii. Fe HC1 NO2 i. NaOH. H,O v. HONO. 0-5°C vi. HyPO2 CI Br Br...
why (b)? explain in detail of the thought process of
how the answer came to be. point out how to use the periodic table
on this one if it can be used.
I am just super confused.
. Refer to Ch. 18 Values. Which response contains all the salts whose aqueous solutions are acidic, and no other salts? I. IV. NH4NO3 II. NaCN III. КСІ NH Br Lici VI. CaCl2 VII. CH,NHẠC VIII. KNO2 IX. NHACH3COO a. b. c. d....
When Cl2 adds to cyclopentene, which product(s) is(are) observed? Cl2 СІ C1 H CI AH H PH n 41C1 C1 "ICI СІ 11C1 H CH H CH 1 II III IV a. I and II b. I and III c. I and IV d. II and III e. II and IV f. III and IV 8. All are formed What is the major Organic product of the following reaction? HCI (excess) -CC СІ H H c1 CI CI (a) H...
(a) Draw and label with required reagents, the reactions of conversion of an alkene into: i. Alcohol ii. Aldehyde iii. Ketone iv. Carboxylic acid v. Epoxide vi. Gem diol vii. Alkyl halide viii. Alkyl dihalide Where appropriate, show the correct stereochemistry of the final products (b) Draw and label with appropriate reagents the carboxylate reaction series
does anyone know the mechanism for this entire thing. i have
part
Scheme I Magnusson Wilson HO i, iii OOH OH v,v 0 vii viii viii hirsutene,1 a (i) CH,-CHMgBr/THF/0°C, (ii) CH3C(OEt),/Hg(OAc)2/ CH,CH,CO,H,ii) KOH/H20, (iv) (COCI),/hexane, (v) CH,CHN2, (vi) Cu(acac),/benzene/A, (vii) 580 °C, PbCO coated glass, (viii) H2/PtO2, (ix) CH,PPh),1-/n-BuLi/Et,0, (x) RhCl,/EtoH/A.
"ОН Step 1 Fill in the following reaction scheme based on the Roman numerals provided below: но Η Ν. HO HOH НО-Н Step 2 H-OH H-OH H ОН HO -Η HO -H НО. H HOH HO -H HO+H CH, OH CH OH CH OH Step 3 HCN cat. HCI H,0 HIO NH,OH NaBHA EROH - 11 III IV V NaOCH, Bra H.0 VII cat HCI CH,OH но" Pa/Baso Hy XI VI VIII х HNO H.O heat XI H,02 Fox(50) XII...
Which of the following reaction conditions would specifically target the anomeric carbon of the pyranose below: OH CH OH 20 НО. он HO cal. HCI H20 PaC, H2 II BnBr, NaH DMF, heat III TBDPSCI AgNO, IV HIO CH,COCH, cat. H,SO V cat. HCI CH,OH VII Pd/Baso H VIII VI O VI O O O VII O IV OV VII
Which of the following molecules has the most acidic alpha hydrogen(s)? - So Lion H OEt OH II III IV H Н EIO OEt HO OH V VI VII VIII
3. Show that (a XOR b)' =a XNOR b. 4. Complete the always procedure for the provided combinational equations: i. m =j' ii. n=jk iii. module UpdateDisplay(j, k, m, n); iv. input j, k; v. output reg m, n; vi. vii. always @ (_ ) begin viii. m j ; ix. n=j&k; x. end xi. endmodule i. t= v's'm' ii. module SetTimer(s, t, m, v); iii. input v, s, m; iv. output reg t; v. vi. always @s, viit =-...