Q: d) H3PO4 + 5 HBr PBR5 + 4 H2O e) 3 Fe(OH)2 + 2 H3PO4 Fe(PO4)2 + 6 H2O f) 2K + Br2 - 2 KBr
A: Given :- a) H3PO4 + 5HBr → PBr5 + 4H2O b) 3Fe(OH)2 + 2H3PO4 → Fe3(PO4)2 + 6H2O c) 2K + Br2 → 2KBr…
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Q: Br -OC(CH3)3 а. b. -OCH,CH3 CI CI с. "NH2 (2 equiv)
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A: Given,
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A: Given
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Q: Teaction Br (CH, CH,CH, );CUU II. I. IV. III. V.
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Q: Suggest a suitable series of reactions for carrying out each of the following synthetic…
A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…
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A: The detailed mechanism provided in attach image
Q: d) H3O* CH3CH2CH=CHBR Mg CO2 -> e) C6H5CH=CHC=N LIAIH4 -> f) Cro, Br H Br
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Q: Br CI CI Br AIC1, Br NBS, A Brz H2SO4, A H2, Pd/C tert-BuO NaBH4 H3O+ peгoxide FeBr3 Group 2
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Q: CH3 [1] CO2 a. CH MgBr [2] H,O+ CH [1] CH,CH,MgBr b. [2] H,O [1] CeHsLi CHO C. [2] HO
A: Here I have solved the top three parts with mechanism
Q: 3)b. FePO4*6 H2O d. CUCN f. CuSO4 * 5 H2O h. Sn(SO4)2 j. Mn(CH3CO2)2 1. Hg(NO3)2 * H2O n. CRSO4 *…
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Q: CHO Meo PPh OMe Brz (1 eg) AIBr3 CO,H 1) Na, NH3(), CH,OH 2) H3O* OMe 1) NANH,. NH3 (1) 2) H,O* 1)…
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Q: نقطتان )2( In the following image these * two compound CH,CH, C=C `CH,CH, CA) H CH,CH, CH,CH, C=C H.…
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Q: CH CH, H Pd/C он CH,CHCH,CH, H,SO, Br "OCH,
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Q: (d) Br (e) CI NaBr ? CH,OH ? DMSO (f) dilute (CH3),COK (g) OTs ? ? Ethanol ŌTs (CHJ,COH
A: Solved in details in step 2.
Step by step
Solved in 2 steps with 1 images
- d. e. (Z) (H3C)2N. OCH3 CNReagents available f. PBr3 g. Mg, ether a. CH3CH,COCH b. C6H5 COCI c. AlCl3 d. NaBH₁, ethanol e. H₂SO4, dil am h. H₂SO4, conc i. SOCI₂ j. C6H5 CNReagents a. C6H5CHO b. NaOH, ethanol h. BrCH2CH=CH2 i. Na* OEt, ethanol j. Br2, H* k. K* t-BuO c. Pyrrolidine, cat. H* d. H2C=CHCN e. H3O* f. I. CH2(CO2ET)2 -CH2CH2CN LDA m. heat g. ELOC(=0)CO2ET Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).
- Reagents Available g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 i. BrCH2CH2Br, Он j. CH3CH2CI, AICI3 k. RCO3H I. H3O* a. CH2=CHCH,CI, AICI3 b. CH2B12, OH c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4 f. K* tBuO Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol). Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.d) e) H₂CN NH ره b ...ОН OH H CH₂ 1. (CH3)₂CHMgBr, ether 2. NH,C1, H,O .CH, CH₂OH Products Products "c H Br. ü OH H ¹0 CH₂ شده NH Br. oły OH OH CH₂ CH,Provide structures of the reactant/products: 1. MgBr 1. KCN a) 2. Нзо" 2. H30* 1. CH;ONa 1. NABH4 2. H30* 2. H30* 6) COOt Na OEt .cOOEt H20* 1. NaOCH2CH3 2. Нао
- Please help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank youRank the compounds by DECREASING reactivity towards nitration with HNO3/ H2SO4 (most reactive on the left). NO2 CH3 II III IV O A. V>V>I> || > || O B. V>I> III > || > IV oCV> || >1> V> I| O D. I > V> > || > IV O E. II > V >1> [IV >| Moving to another question will save this response. Co searchDraw the organic prouduct of the reaction with a) HBr b) Br2 c) H2, Pt/C d) O3; (CH3)2S
- a) b) c) d) CI H3CH₂CC CH CO + CH3MgBr 1. 2 eq. PhMgBr 2. H3O+ 1. NaNH, 2. PhCHO 3. H₂O* Azculi + 1. ether 2. H30* -Br r2. Which of the following is NOT an organometallic compound? A. CHỊCH,CH,Li (CH₂)₂Zn D. K [O-C(CH₂))]¯ B. (CH₂CH₂) Pb C.Compound A produces compound E in four steps. What is compound A? A a B b C C D d E e Br 1) MeMgBr H2Cr207 1) `MgBr H2SO4 (conc.) 2) H20 2) H20 NaBr Possible starting materials OH H. HO. a) b) c) d) e)