HN03 A, CEN H2504 HN03 b. H2S04 Give the products Jor the above KIs. Do each thes of reoctions go farter or slower than Berzene as a storting ma terial ?
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A: Rate determining step is the slowest step of reaction .
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Q: Iny the expected major Ving Teaction. H2SO4 1-methylcyclohexene H20 O a. Но b. Но c. HO.
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Q: Determine the product of the ff. rxn НО H2SO4 А. C. D. All of the given choices B.
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Q: Br2 (g) FeBr3 CI CI Br2 H2NNH2 В C (h) A FeBr3 AICI3 OH (Give all products) NH2 HNO3 (i) H2SO4
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Q: Name each alkene and specify its configuration by the E,Z system.
A: This given alkene has configuration :
Q: ! wite Out He stepwie mechanism, including intermediaves or 1. transition state for : Na oH > Br.
A: The given compound is reacted with base to give alkene compound.
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Q: Draw the products of each reaction, and indicate the stereochemistry where appropriate.
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Q: which is the best leaving group? explain why. A)C6H5CH2Cl B)C6H5CH2Br C)C6H5CHCl2 D)C6H5CHClBr…
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Q: 1. Provide the products for the given reaction. Give the stereochemistry (cis/trans) of the product…
A: Answer Provide the product for the given reaction with…
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Q: 2. Arrange the structures below in terms of most stable to least stable. Ans a. A B b. Y Ans
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A: More is the acidity of leaving group , better is leaving group .
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- In which species (NO3- or CH3NO2) are the N-Obond(s) longer? In which species (NO3- or CH3NO2) are the N-Obond(s) weaker?What is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. Atrans-2-Butene is more stable than cis-2-butene by only 4 kJ/mol, but trans-2, 2, 5, 5-tetramethyl-3-hexene is more stable than its cis isomer by 39 kJ/mol. Explain.
- How can X be prepared from a constitutional isomer by a series of [2 + 2]cycloaddition reactions? Interest in molecules that contain severalcyclobutane rings fused together has been fueled by the discovery ofpentacycloanammoxic acid methyl ester, a lipid isolated from themembrane of organelles in the bacterium Candidatus Brocadiaanammoxidans. The role of this unusual natural product is as yetunknown.Assign R or S configuartion to the following molecules.Draw the product formed when diene M undergoes disrotatory cyclization. Indicate the stereochemistry at new sp3 hybridized carbons. Will the reaction occur under thermal or photochemical conditions?
- Draw the product formed when diene M undergoes disrotatorycyclization. Indicate the stereochemistry at new sp3 hybridized carbons.Will the reaction occur under thermal or photochemical conditionsWhat is the expected major product of reacting cyclohexane carbaldehyde jwith CH3NH2?Elimination occurs when (Z)-3-bromohex-3-ene is treated with NaNH2. Under the same conditions, 1-bromocyclohexeneundergoes elimination much more sluggishly. Explain why
- For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOC(CH3)3 in (CH3)3COHWhich of the following would accomplish the transformation below? a) 1. HSCH2CH2SH, H+; 2. H2, Raney Ni b) H2N-NH2, NaOH(aq), heat c) H2, Pd d) All of the aboveArrange the following compounds in the increasing order of reactivity towards Conc.HNO3 & Conc.H₂SO4 1. Benzene 2. Chlorobenzene 3. phenol 4. Toluene 5. Nitrobenzene A 1.2.3.4.5 (B) 5.1,243 5.1.4.2.3 D 5.2.1.4.3