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…
A:
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.
A:
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.
A:
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
A:
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
A:
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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- 3. Which carbon would the Br of HBr add to in the following unsymmetrical alkenes? 1 Problem Set #7 Chemistry 227 а. b. С. d. H3C H3C е. H Н. H3C. TH. CH3 H H H the C=C in the ring do not react with H*1. Help me determine the IUPAC name of these compounds, please because I can't still understand how to get their IUPAC names. Thank you! а. b. C. HO d. Br BrWhich structure is different from the following? * HCH3 CH3 CH3 a) CH3 CH, CH, b) H H3C- CH3 CH3 H H CH3 CH3 H. H. CH3 d)
- 1. Draw the structure for each compound. a.(3R)-3-methylhexane b. (3R,5S,6R)-5-ethyl-3,6-dimethylnonaneQ1. How would you SXatbesize the following substances starting from benzene? Draw all the reagents and intermediate structures but you do not need to draw any curly arrows. Assume that you can separate extbe and para isomers, if necessary, and note more than one step is required. NO2 NO2 Br Br2. Consider the following organic molecules A-H. Many of them are natural products isolated from Nature. Please answer the following questions by writing the Letter pertaining to each molecule next to the question. -N- H;C "CO,H N. Но CH2 ČH3 B strychnine (a plant alkaloid) hirsutic acid A nepetalactone (essence of cutnip) (a fimgul metabolito) H- H. I CH,0 E helminthosporal (a imgal toxu) D progesterone F cantharidin (a progestin hommone) (am insect vesicant) Br NO2 Br CI G untenine C (E)-1,6-dibromo-2,7-dichloro-3,7-dimethyloct-3-ene (fom red algae) (4 sponge metabolite)
- 1. Provide proper IUPAC names for the following compounds. a. CH3 | CH3C CCHCH2CH2CH3 CH3 Br b. H₂C=CH-C-CH-CC-H | CH3 C.Convert each compound to a skeletal structure. a. CH3(CH2)7CH3 window open b. 1,1−diethylcyclohexane draw structure ... c. (CH3CH2)2CHCH2CH2CH3 draw structure ...3. Compare the compound at right to pinitol. is it a A conformer H- H. CH,OH ® structural isomer C geometric isomer H OCH, D. none of the above of pinitol? For each alternative, explain why you made the choice that you made here. VWhy or why not? D.
- Which structure is different from the following? a. b. C. d. CH3 н Н CH3 H CH3 CH3 H3C- н CH3 CH3 н H CH3 н Н н CH3 н H Н -CH3 CH3 CH31. Using IUPAC guidelines, name the following organic compounds. Answer5) Use compounds X, Y and Z (shown below) to answer the following questions. H. H3C" "CH3 ОН CH3 compound X compound Y compound Z a) Is compound X classified as cis, trans or neither? b) Is compound Y classified as E, Z or neither? c) Is compound Z classified as R, S or neither? d) Are compounds X and Y constitutional isomers of each other? (YES or NO) e) Are compounds Y and Z constitutional isomers of each other? (YES or NO) f) Classify compound Y as a primary, secondary or tertiary alcohol. g) Which compound(s) is(are) chiral? h) Give the IUPAC name for compound Z, omitting the absolute configuration (R or S) designation. i) In the indicated spaces below, draw stereoisomers of compounds X, Y and Z. stereoisomer of compound X stereoisomer of compound Y stereoisomer of compound Z