Q: Balance each reaction and write its reaction quotient, Qc:
A: A balanced equation is that which consists of an equal number of atoms on either side of the…
Q: A. [FeBr(NH3)2(H2O)][Cu(CN)4] = %3D B. [PtBrCI(SCN)(H20)][AgCl2] = C. [Zn(H20)4]a[ZnCl(OH)2(S2O3)]2…
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Q: OH CH3 H3C H3C OH CH3 O: H3C CH,(CH,),,CO,H CH,(CH,),CH=CH(CH,),CO,H (CH,),CO,H H. C=C (CH,),CO,H…
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Q: 1. NaOC(CH3)3, HOC(CH3)3 Br 2. B(CH3)3
A: The alcohol functional group in a molecule is identified by the presence of R-OH group in the…
Q: NO2 n-BuSO CFa NaH, DMF, rt 47% ON Meo Meo
A: Here we have to write about above reaction-
Q: 2 CHJCOH он 3 1B HE Lindiar's PIO 1D 2 Ether HB KMno, G 1A 1 1C OH HO H F. mCPBA
A: We have to complete the given reaction map with the given choices.
Q: 1.) 2.) CH3Br NH 3.) H3O*, H20 molecular seives (i.e. - H2O) a) 1.) b.) 1.) c) 1.) H. H. 2) 2) 2)…
A: Correct option is (a)
Q: CH,CH,CH,NHCH, ? HO* CHO ? 6. 7. ? Zn, H,O* + 5.
A: Given,
Q: a) CN H,O, H* CH3 OH b) H3C- CH3 c) CH3 KMNO4, A, H,0* CH3 d) Br Mg, éther CO, H*
A: The given organic transformations are examples of the formation of the amide, anhydride, oxidation…
Q: (a) MnO,¯ + Vo²* → Mn²* + V(OH),“ (b) I2 + H,S(g) →T+S(s) (c) Cr,0,²- + U+ → C** + UO²+
A: Since you have posted a question with multiple sub-parts, we will solve the first three sub-parts…
Q: Draw the organic products formed in each reaction.
A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…
Q: F3C Br2, Fe A HNO3, H2SO4 В NO2 HNO3, H,SO4 Br2, Fe NO2 C HO3S' D H3CO
A: The above given reactions are aromatic electrophilic substitution reactions, in which benzene ring…
Q: Draw the organic products formed in each reaction.
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Q: Br Br A) B) O2N. NO2 D) CI NO2
A: Given that : We have to give the IUPAC name of the following compounds :
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…
Q: Brz/H,0 H = В + С
A:
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
A: Intramolecular Friedel-Crafts Alkylation The nucleophile is the aromatic ring, and the electrophile…
Q: d. [Cr(H2O);Br]2* • e. [Cu(NH,CH,CH,NH2)CI,J?- •f. [Fe(OH),] е.
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Q: XEF4 H2S NH2F CBr4 PCI5 H2CO NO3 BF3 CO2 IF2 А C E F G J ou only need to provide a single answer for…
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Q: CH — сH, — сн,— сн — сн, — сн, CH;
A: selection of longest carbon chain i.e. the principle carbon chain numbering (substituents get the…
Q: HBr H₂O₂ hv 1) NaNH, NH3 2) CH3Br
A: There is more than one question,and as per answering guidelines I can answer first three…
Q: H,0 I. DIBAL-H OCH CH, 2. H,0 CH,CH;NH, 1. CH,MgBr 2. H,O CH,NH, LO 2(CHS
A:
Q: What are the products of the following reactions?
A: Solution:- (a)
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: Pd(OAc)9, 2 PhgP 2 C,H;CH=CH, + I- I (CH;CH2)3N
A:
Q: Complete these Heck reactions.
A: The Heck reaction is completely stereospecific with regard to the haloalkene; the configuration of…
Q: (CH),CuLi CH3 b) HOCH,CH,OH CH3 c) H,NNHC,H, HC. CH3
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Q: он a) CH,CH,CHCH3 H2SO, isi NANH2 b) CH,CHCH,CI NH, c) CH,CH=CCH,CH3 HBr
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Q: (a-b) 1. Br₂, H₂O 1. KOH 2. KCN, H2O
A: 1. Alkene with addition of Br2 / H2O gives bromohydrin further by using KOH it is converted into…
Q: The molecules below are: H F H H. F F'H F
A: First, let us observe the given structures. The given structures have the same number of atoms and…
Q: (а) Et HBr (0 (b) AICI, H;NNH, (i) H,C. KOH, HCI CH, ö H3C (v) (iv) (iii) AICI, (c) +] MeO (vi) CH3
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Q: H,O(g) + CH;OH(g) CO2(g) + 3H2(g) H2O(g) - 228.57 - 241.82 CH;OH(g) 161.96 CO2(g) - 394.36 - 393.51…
A: We will calculate Kc and Kp both with the help of Delta G0 value. Kindly check the complete…
Q: P3(g) S(s) + O2(g) → SO2(g) A;H°;(SO2,g) = -297kJ/mol 2 SO3(g) → 2 SO2(g) + O2(g) AH°2 = 198KJ/mol D…
A: We have ∆H value of two reaction and calculate for other equation so we have to do experiment with…
Q: но- CEN HO -CEN HO,
A: Phenols are the compounds that contains a benzene ring containing a directly bonded -OH group. These…
Q: CO,Et HO (1 equiv) NO2 NO2 a.) b.) c.) ON NO2 NO2 -NO2 CO,Et ON NO2 co,Et e.) CO,Et CO̟E! O,N- NO2…
A: First step of this reaction is formation of carbanion. And 2nd step is ipso substitution.
Q: 11) CF, + Br, O_CBr, + F2 - - 12) K+ MgBr O KBr + Mg 13) Na + NaOH + H2
A: Balance the following chemical reaction by hit and trial method.
Q: он H2SO4 ? a) H,SO4 ? b) HO OH H,SO, ? c)
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Q: S0,] -| M CH20] = 2 M • Constuct (CE Table Given: %3D Find ko. SO3 6) + H20 9) 今 H2SO4
A: Given Reaction is - SO3(g) + H2O(g) ----> H2SO4(g) And, concentration of Reactants are - [SO3]…
Q: 4. HFag) 2 Agʻaq) + Znu C2Hlg + Ozia) 5. 2 Ag + Zn²*taq) 6. 2 C2Halg) + 2 H;O 7. Cu + 2 Hzig CHag 8.…
A: let us consider a general reaction, aA+bB→cC+dD The equilibrium constant for a given reaction is…
Q: P4 + H2 > PH3 a Fe2O3 _C → Fe CO2 + + C,H10 O2 CO2 + H2O
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Q: Br HNO3 H2SO4 Br Br Br Br Br NO2 SO3H `N½CI SO3H `NO2 ÓH ÓH ОН Он ÓH (a) (b) (c) (d) (e)
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Q: Draw the constitutional isomer formed in each reaction.
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Q: A. Hz Si Glz t Ha0 → He Siy Og + HGI B. (NH,); POy + Pb(NOS)y → C. Hg (OH), + H3PO4 Pb, (PO4), +…
A:
Q: КCN b HCI LAH a H2SO4 Heat CgH,O2N CeH1403
A: 1) substitution 2) CN to COOH 3) Reduction to alcohol
Q: НО HNO3, H2SO4, Br `NO2 H2SO4
A: Answer of the question given below,
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.
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- A. For each pair of compounds, fill in the appropriate information needed to distinguish them.(attached) B.Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.1. (d) Provide a name for each molecule (I narrowed it down to three subparts)
- I'm looking for an alkene with a single methyl group and an anti markovnikov Br at the last carbon and the markovnikov with Br on the bottom. The image is attached is just to illustrate positioning of the Br, and not an actual alkenePlease help with parts a-cWill the cyclopropane formed be facing same direction as substituents or away?(will it have dashed wedges)?
- Please explain how it forms an alkene? I am the problems and my CH3s keep aligning like in question "a", when they should be anti to each other? Please explain how they are suppose to form? Thank youHoew manyy allylic carbons are there? explainAnswer the following question about compounds A–D (See in attachment) Label each compound as a cis or trans isomer