The following scheme shown will lead to formation of which major product from benzene? [6] . HNO3 H₂SO4 Product A. P-Bromonitrobenzene B. Meta-Bromoaniline C. Meta-Bromonitrobenzene Br FeCl D. None of the above options is correct
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![The following scheme shown will lead to formation of which major product from
benzene?
[6]
HNO3
H₂SO4
Product
A. P-Bromonitrobenzene
B. Meta-Bromoaniline
C. Meta-Bromonitrobenzene
Br
FeCl3
D. None of the above options is correct](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ffe29ad59-4fd5-48c7-89f3-7f0378eab9d4%2F8951ac63-1d57-4f76-9488-8dfd79d77653%2F0ajmwq_processed.jpeg&w=3840&q=75)
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- 6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HOThe following scheme shown will lead to formation of which major product from benzene? HNO, Br Product H,SO, FeCla O A.P-Bromonitrobenzene OB. Meta-Bromoaniline OC Meta-Bromonitrobenzene O D. None of the above options is correctb. Provide mechanisms and/or products for the following transformations. Pd°Ln, Cul, PhBr 1. HBpin, THF ? EtzN, THF 2. Pd°Ln, PhBr, H. K3PO4, H2O/THF
- can you explain how can we determine major and minor product from these reaction elimination-addition? &=&=1561=6, NH₂ majo CH, NH₂ NH₂ &=-&-&-& majo CH3 OCH, CI NINH, NH 3liq. KNH₂ NH309. Br ΚΝΗ, NH CI CH₁ 80 80 OCH, majo NH, NH₂ mino CH3 mino NH₂ NH₂ NH, NH, CI majo CH3 majo NH₂ NH₂Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?Arrange the following alkyl bromides in order of INCREASING reactivity towards SN2 reaction. I. 1-Bromohexane II. 1-Bromo-2,2-dimethylbutane II. 1-Bromo-2-methylpentane IV. 1-Bromo-3-methylpentane III < || < IVWhich of the reactions shown would produce isopropylbenzene as the major product? AICI3 H₂SO4 ||| OH H₂SO4 || AICI3 IVMy Home OWLV2 | Online teaching and lear X G D /ilrn/takeAssignment/takeCovalentActivity.do?locator=assignment-take IReviaw Toples Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. You do not have to consider stereochemistry. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate multiple reactants using the + sign from the drop-down menu. aste [F ChemDoode Submit Anewer Retry Entro Group 8 more group attempts remainingProvide a plausible arrow pushing mechanism for the reaction below. Os-OtBu 's-OtBu HN 1. LDA 2. OMe SO,Ph 3. aqueous workupMechanism. Propose a mechanism for the following reaction. Label the rate-determining step and the major resonance contributor. Make sure to include (1) the formation of the electrophile and (2) all significant resonance contributors of the sigma complex intermediate. NO2 H2N H2N. HNO, (1 eq.) H2SO4 O °C CF3 CF31. .CI HC C: Li HC CH LICI 2. -CH3 OH Aqueous HO-S- -CH3 acetone g = SN1 Nucleophilic substitution Electrophilic a = Proton transfer addition h = SN2 Nucleophilic substitution b = Lewis acid/base e = El Elimination c = Radical chain f= E2 Elimination substitution Identify the mechanism by which each of the reactions above proceeds from the mechanisms listed. Use the letters a - i for your answers. among 1. 2.Which synthetic route(s) would complete the reaction shown? Br || ||| I and II O I and III ? HO OH + enantiomer Synthesis I: 1. NaCCCH3; 2. Na/NH3(I) ;3. OsO4; 4. NaHSO3, H₂O Synthesis II: 2. NaCCCH3; 2. H2, Lindlar's catalyst; 3. MCPBA; 4. aq. H₂SO4 Synthesis III: 1. NaCCCH3; 2. H₂, Pt; 3. MCPBA; 4. aq. H₂SO4SEE MORE QUESTIONS