Nucleophilic Aromatic Substitution Draw the curved arrow reaction for this experiment showing the formation of two possible products: 2-chloro-1-methoxy-4-nitrobenzene 1-chloro-2-methoxy-4-nitrobenzene
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- Please I need help with this question Based on the experiment- Synthesis of Iodosalicylamide – An Electrophilic AromaticSubstitution (a derivative of benzene, salicylamide was used and substituted an iodine atom onto the ring; the ring is the nucleophile while the atom/molecule that is being substituted onto the ring has anelectrophilic character) Please I need help with this QUESTION: Draw the structure of the final product(s) based on the ATTACHED IR analysis. Also label the signals (both the frequency and molecular motion) that help determine the final product(s). Thanks in advancePlease help me with the organic chemistry problem below: Consider the reaction below: (Check the attached image) (it is between Furan and maleic anhydride, a DIels-Alder reaction) a) Will this reaction for an endo product (with a melting point of 80-81 degrees) or the exo product (with a melitng point of 114 degrees)? b) Carefully explain why the product must have been formed the way it did (exo or endo). c) Provide a mechanism for this reaction.Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Draw all the oissuvke resonance forms of methoxybenzene, including the hybrid Based on the structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.
- Draw an electrophilic addition reaction of a conjugated diene that produces more than two organic products (show ALL products)TRUE OR FALSEThe reaction below exhibits electrophilic aromatic substitution:The compound below has multiple electrophilic sites which could potentially react with an organolithium reagent, like phenyllithium. If only 1 mole of Phli is added for each mole of starting material, which atom is most likely to be attacked by the nucleophile?
- Please answer both parts to the questions completely. I will rate the answer afterwards. For a diels-alder reaction between anthracene and maleic anhydride, are the exo and endo forms of product 9,10-dihydroanthracene-9,10-ɑ,β-succinic acid anhydride different stereoisomers or are they the same molecule? Explain your answer by drawing the molecule. Would it be favorable to get a 1,4-adduct of anthracene and maleic anhydride? Why or why not? If the 1,4-adduct of anthracene and maleic anhydride had formed, would it have different exo and endo isomers? Yes or no and why?Construct a three‑step synthesis of 1,2‑epoxycyclopentane from cyclopentanol by dragging the appropriate formulas into the bins. Note that each bin should hold only one item, and not all of the given reagents or structures will be used.Below 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?
- Please provide 3 possible mechanisms for bromination of trans-cinnamic acid and pyridinium tribromide (Br2) with stereochemistry (wedge and dash bond) (1 for anti addition, 1 for syn addition, and 1 for 50:50 syn and anti additon).By which substitution mechanism (SN1 or SN2) did the reaction occur? How did you know? For what reason does the substitution occur at only one of the bromine atoms, and in particular the bromine atom that it did?From 1 being the slowest and 4 being the fastest rank the aromatic hydrocarbons in terms of increasing raters of nitration via electrophilic aromatic substitution