Which benzene derivative would be the most reactive in an electrophilic aromatic substitution reaction? Click on a letter A through D to answer. А. `NO2 C. В. OH Br D. B.
Q: SCH3 OCH3 Br N(CH3)2 1 2 3 A) 3>1> 2>4 B) 3> 2>1>4 C) 4 > 2 > 3 >1 D) 1>3> 2 > 4
A: Order the carboxylic acid derivatives from most reactive to least reactive towards nucleophilic…
Q: Which is most reactive in electrophilic aromatic substitution? (A) (B) CH3 (C) CF3 (D) OCH3
A: Rate of Electrophile aromatic substitution increase as density of electron increase on benzene ring…
Q: Label the reactive features of each molecule and then circle the nucleophile used in the reaction…
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Q: Indicate which of the ff. statements regarding nucleophilicity is incorrect. A Second row elements…
A: As we goes down the group nucleophlicity increase and basicity will decrease . This fact can be…
Q: 19 13 10 20 15 18 11
A: HOMO-Highest occupied molecular orbital and LUMO is the lowest unoccupied molecular orbital. Both…
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Q: Why do we need to use lewis acids before electrophilic aromatic substitution reaction proceeds? to…
A: Why do we need to use lewis acids before electrophilic aromatic substitution reaction proceeds? The…
Q: Which halogens are attached to Vinylic carbons? 2. Which of the following is the best electrophile?
A: The formula of vinylic functional group is shown below: -CH=CH2. The group which contains ethylene…
Q: Which is least reactive in electrophilic aromatic substitution? (A) (B) CH3 (C) CHO (D) C3
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Q: How to Form an Internal Alkyne by Two Sequential SN2 Reactions ?
A: The terminal alkynes are those alkynes in which the triple bond is present between the first and the…
Q: For each horizontal row of substituted benzenes, indicatea. the one that is the most reactive in an…
A: Various types of mechanism are studied in organic chemistry. Different organic compounds undergo…
Q: Which one of the statements below is wrong about Zaitsev’s Rule. a. None of the above
A: Zaitsev's rule help us in predicting that which alkene product is favoured in elimination…
Q: Rank group of compounds from most reactive to least reactive toward electrophilic aromatic…
A: When the benzene ring has electron-donating groups, then the benzene ring has more reactive to…
Q: What is the appropriate electrophile nucleophile and solvent to achieve this final product
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Q: Explain why a nucleophilic reagent such as ethoxide adds to an alkyne more easily than it adds to an…
A: The unsaturated hydrocarbons are of two types namely alkenes and alkynes. The alkenes consist of at…
Q: Generally alkynes prefer to undergo: SN2 Both SNI and SN2 SNI Addition Reaction
A: Alkynes are unsaturated system (due to the presence of multiple bonds in them). So, their principle…
Q: Which benzene derivative would be the most reactive in an electrophilic aromatic substitution…
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Q: Halohydrin formation from an alkene involves: a. Temporary induction of the dipole moment of a…
A: Halohydrin is prepared from Reaction between alkene and halogen in presence of water Molecules.…
Q: Good nucleophiles that are weak bases favor substitution overelimination. Explain this ?
A: Good nucleophiles are weak bases which favor substitution often.
Q: Aliphatic aldehydes have slower rate of reaction in comparison to aromaticaldehydes. *
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Q: Why does bromination give exclusively anti products while chlorination gives a mixture of syn and…
A: Halogenation is the addition of halogens to alkenes. Halogenation usually gives anti products. If…
Q: Which of the following could act as a nucleophile?
A: Given:To give which of the following could act as a nucleophile
Q: Which of the following are anti-aromatic? Furan b. Thiophene С. H Pyrrole d. Pyridine e. None of the…
A: Conditions for an organic compound to be aromatic: The organic compound must be 1. cyclic 2. planar…
Q: How many carboyxlic acid groups will be attached to the benzene ring after the reaction? KMNO4
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Q: Without reading ahead in L Chapter 20, state whether it should be possible to carry out each of the…
A: The reactivity of the acid derivative depends on the partial positive charge on the carbonyl carbon…
Q: what is the Mechanism and important examples of aromatic Nucleophilic Substitution reactions
A: The substitution reaction which take place on an aromatic ring via nucleophile.
Q: 10. Use multiple steps to complete the synthesis below. ОН Br
A: Bromo alkane forms grignard reagent on reaction with Mg metal in dry ether medium. Alkyl group of…
Q: [Review Topics] [References] Indicate, by letter(s), the position(s) on the ring at which…
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Q: Indicate which of the ff. statements regarding nucleophilicity is incorrect. 1. F- is more…
A: Nucleophilicity is directly proportional to Polarisability. Order of nucleophilic halide :…
Q: Rank the relative reactivity of nucleophiles. The shortest time means fastest reaction, which gets…
A: To arrange the nucleophile in order of reactivity.,
Q: Which position(s) on the ring would substitution occur when the aromatic compound shown undergoes…
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Q: a) This alkene can be prepared via Wittig reaction. Draw structural formulas for the aldehyde and…
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Q: Why some substituents make a benzene ring react faster than benzeneitself (activators) ?
A: Directive influence of the attached substituents on the benzene ring The ability of the attached…
Q: Explain the Limitations on Electrophilic Substitution Reactions with Substituted Benzenes ?
A: Electrophilic Substitution reactions are the most important and characteristic reactions of Benzene…
Q: ophilic aromatic substitutions proceed in two stages. 1. Attack of the aromatic ring on the…
A: Here the step 1 Is generation of an electrophile which is generated as the Br-Br bond interact with…
Q: = most reactive toward electrophilic aromatic substitution?
A: Compound which is more electron rich is considered to be most reactive towards electrophilic…
Q: In electrophilic aromatic substitution, what happens during the first step of the reaction? A)…
A: In general electrophilic aromatic substitution reaction involves two steps. Step 1 : nucleophilic…
Q: prevent the occurrence of radical chain explosion
A: According to the question, explosions occur when the rate of reaction increases dramatically over a…
Q: why a CH3 group directs electrophilic aromatic substitution to theortho and para positions ?
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Q: type op or m, to indicate if the group would be an op or meta director in electrophilic aromatic…
A: Displacement of pi or non bonded electrons through conjugation is called mesmeric effect
Q: How would you convert the benzene into cinnamic acid?
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Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…
A: Naphthalene undergoes electrophilic aromatic substitution in the first position. The structure of…
Q: answer....given below some compounds give the rank most reactive to least reactive in an…
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Q: When a is on an atom directly attached to a benzene ring, the benzene ring will stabilize it by…
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Q: Rank group of compounds from most reactive to least reactive toward electrophilic aromatic…
A: The order of decreasing reactivity toward electrophilic aromatic substitution is,
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- Decide which compounds from the list below are best suited for nucleophilic addition reactions and which ones are more appropriate for nucleophilic substitution reactions.Draw curly arrows to show electron flow in the last step of the aromatic bromination reaction below.17. Which aromatic compound in figure 17 will be least reactive in an electrophyllic aromatic substitution reaction?
- While CH3OH is the solvent in the reaction, and a nucleophilic one, why doesn’t CH3OH act as the nucleophile in this reaction?When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,
- Alkyl halides act as what in substitution reactions? Nucleophiles Electrophiles Catalysts Product E2 is bimolecular which means: both the nucleophile and the product take part in the step whose kinetics are measured both the nucleophile and the alkyl halide take part in the step whose kinetics are measured both the product and the alkyl halide take part in the step whose kinetics are measured None of the abovewhy a CH3 group directs electrophilic aromatic substitution to theortho and para positions ?A benzene ring reacts with these reagents in order: 1) Cl2, AlCl3 2) Mg 3) CH3CH2CHO 4) H + 5) conc. H2SO4, heat, -H2O I am confused about what happens after the first step.
- Which of the following species are likely to be nucleophiles and which electrophiles? Wich might be both?Complete the following reaction schemes. Some may take more than one step and some may have several routes to the product.Draw the appropriate reagents/ solvent above and below the arrow necessary to conduct the following reactions.