2. Are the methoxy groups on benzene likely to direct substitution to the ortho and para positions, or the meta position. Justify your answer.
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A: Cis- and trans-isomerisation of stilbene can take place as photo-chemical isomerisation.
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A: The correct answer is given below
Q: a) N.
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Q: a) Draw all curved arrows that show the entire transformation of 1 into 6, and identify the entire…
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Q: 4. Are there any RX compounds from part A that are not expected to undergo an Sn1 or SN2 reaction?…
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Q: Show how the p orbitals overlap to generate the n4* of cyclobutadiene. Which would have a smaller…
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Q: A Moving to another question will save this response. Question 5 Which one of the following…
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A: Alkyl halides are the organic compound in which carbon is attached with halides, F, Cl, Br, I.
Q: true or false of these three potential leaving groups (-OH, -Br , and -OCH3) , -OH is the poorest.
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Q: 2. Above is S-adenosylmethionine (SAM). Note that R'-S-R is a very good leaving group. You do not…
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Q: List the Unimolecular substitution (SN1) mechanistic steps (as discussed in the problem solving…
A: The correct explanation with example SN1 reaction is given below
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A: In the sulfonation Reaction, we can used sulfonating agent like SO3, py or SO3 / H2SO4. This reagent…
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A: This can be explained as:
Q: In which case is the indicated unshared pair of electrons not a contributor to the n aromatic…
A: In the following compound the unshared pair of electron do not contribute the π aromatic system.
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Q: In Part 1, select the two new o bonds that were formed in this Diels-Alder reaction. In Parts 2 and…
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Q: Outline the synthetic steps necessary to carry out the conversion below. You may use any organic
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A: Using concept of Hoffman elimination reaction.
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Q: Construct MO energy diagrams for the cyclopropenyl cation, radical, and anion. Which of these…
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Q: Which position(s) on the ring will be most likely to be sulfonated? Explain your reasoning for…
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Q: By which substitution mechanism (SN1 or SN2) did the reaction occur? How did you know? For what…
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A: We have to rank leaving group tendency :-
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Q: Explain why the halogens, when attached to a benzene ring, weakly deactivate the ring toward…
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Q: 4. Which do you think is more chemically stable, the reactants or products of each of the reactions…
A: As all the above process result in production of energy it means all reaction are exothermic.
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- Why does the methyl on the right have higher priority than the ethyl on the right when labeling the molecule as an E or Z isomer?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?Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Which compound below is ideal for a SN1 reaction?
- Can you mark the part of compound 4 that are from compound 2? Also is compound 2 act as an nucleophile or electrophile when it reacted with compound 1?1. State the effects of substituents on a benzene derivative towards further aromatic substitution. 2.Based on the above, suggest the various types of substituents that can be attached to Benzene.Please complete both subpart reactions in clear handwritten answer on a paper!
- Any help with this would be great! Explanations definitely welcome, thanks in advance for any help:) What is the major product of the reactions?How does increasing base, solvent, or alkyl halide or aptly halide + base affect or decreasing them affect the reaction rate for e2/e1 and sn2/sn1? Please provide examplesGive a clear explanation handwritten answer....given below some compounds give the rank most reactive to least reactive in an electrophilic aromatic substitution reaction
- Draw and label the substituent priority on both E-stilbene and Z-stilbene and justify how they are namedAnd how many substitution products would you anticipate?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.