Q: CH3 CH3 1. BH3, THF 2. NaOH, H,O, Н-02 H3C CH2 H3C Alkenes can be hydrated via the addition of…
A:
Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…
A: Given; Reaction of naphthalene with CH3CH2COCl and AlCl3
Q: Draw the structure of a hydrocarbon that reacts with 2 equivalents of H2 on catalytic hydrogenation…
A: Catalytic hydrogenation- H2 can be added across a double bond or triple bond in presence of…
Q: N. cat. H2SO HN H20
A: Given, The structure of products are; and In the reaction, carbocation goes into conjugation.
Q: 1. Which of the following are aromatic? N. N- ZT ZI ZI
A: The compound should satisfy the Huckel's rule to consider it as aromatic. The rules are given below.…
Q: Which one is an electrophile in the nitration of benzene? a) ΗNO b) NO2 c) ÑO3 d) Ňo i. a i. d. ii.…
A: Nitration of benzene involves treatment of benzene with concentrated sulfuric acid and concentrated…
Q: Rank the species in each group in order of increasing nucleophilicity. a. CH,, "OH, "NH2 b. H20, OH,…
A: Since you have posted a question with multiple subparts, we will solve the first three subparts for…
Q: Aromatics can be converted into nitroaromatics upon treatment with a mixture of nitric and sulfuric…
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Q: How many of the following are aromatic? 0000 О Н б
A: For a molecule to be aromatic it must be planer, conjugated, and must follow 4n+2 pi electrons rule
Q: Where does the indicated aromatic system undergo electrophilic substitution? NO2 iv i ii CO2M. ii
A: Aromatic electrophilic substitution occurs at the site where the electron density is maximum.…
Q: Rank the following compounds in order of increasing stability
A: According to Huckel's rule, a conjugated compound is said to be aromatic if it has (4n + 2)π…
Q: 1. The multifunctional molecule below can undergo both nucleophilc addition reactions and…
A: In the given molecule, the free aldehyde group and the free ketone group will undergo Nucleophilic…
Q: Rank the following compounds in order of increasing stability.
A: The stability of the given systems can be solved by the conjugation concept. Conjugation means to…
Q: Which of the following is expected to show aromaticity? CH CH HC CH NH O none of the above is…
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Q: Identify an electrophile from the following list A. CH3- B. NH3 C. BH3 D. None of these
A: Any molecule, ion or atom that is deficient in electron in some manner can act as an electrophile.
Q: redict the product of the following reaction: 1. CH,CH,CH,C=OCI, AICI, 2. Br3, FeBr, 3. Zn(Hg), HCI,…
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Q: Draw the structure of a hydrocarbon that reacts with 2 equivalents of H2 on catalytic hydrogenation…
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Q: Which of the following compounds are aromatic? :N A N B D N-N E F О В, С, F O B, F О В, С, F, G O B,…
A: According to huckel rule , when (4n+2) pi electrons( 2,6,10... etc.) are in complete cyclic…
Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…
A: The major products of the reactions of naphthalene with HNO3, H2SO4 is predicted as follows,
Q: Rank the following substituted anilines from most basic to least basic:
A: Electron withdrawing group present in the phenyl ring increases the acidic strength. This results…
Q: Rank the species in each group in order of increasing nucleophilicity. a. CH3CH2S−CH3CH2O−, CH3CO2−…
A: Since we only answer upto 3 sub-parts we'll answer the first 3. Please resubmit the question and…
Q: Arrange the following alkanes, in order of increasing the reactivity reaction toward halogens in…
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Q: 2- Which of the following is not an electrophile? A) C2H5OC¿Hs В) BF; C) [CH3];C+) D) HỌC
A: An electron deficient species is known as electrophile.
Q: Draw the four resonance structures formed during bromination of methoxybenzene, CH3OC6H5, with…
A: Methoxy group in methoxy benzene is a ortho-para directing group. Therefore, bromination of methoxy…
Q: Rank each of the blue functional groups from least to most deactivating with 1 being the least and…
A: The compounds given are,
Q: When an unsymmetrical Alkenes such as propane is treated with N-bromosuccinimide in aqueous dimethyl…
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Q: Rank the following compounds by their reactivity with CF (1 = least reactive, 3 = most reactive)
A: Ranking against reactivity with Cl-
Q: Which of the following compounds is the most reactive towards electrophilic aromatic subsitition by…
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Q: Which compounds are aromatic? (A) (B) (C) (D) (E) (F) B. (H) (1) (G) H-
A: The following conditions must satisfied in order to becomes aromatic. Must be planar Must be…
Q: Please Prouide the missing Feagents, NH2 Please Prouide the missing reagents. OH Br
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Q: In which solvent—ethanol or diethyl ether—would the equilibrium for the following SN2 reaction lie…
A: The equilibrium reaction provided is shown below.
Q: 2.4 Rank each set of substituents in order of decreasing influence on electrophilic aromatic…
A: In electrophilic aromatic substitution the ease of reaction decreases with electron withdrawing…
Q: Rank the compounds in each group in order of increasing reactivity in electrophilic aromatic…
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Q: Arrange the following compounds in order from the most stable to the least stable.
A: The stability order of the given compound from most stable to least stable can be arranged as,
Q: Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution…
A: Aromatic electrophilic substitution reaction: Aromatic electrophilic substitution reactions are the…
Q: Benzene can be nitrated with a mixture of nitric and sulfuric acids. NO2 HNO3, HSO, Draw the 3-atom…
A: An electrophile is a species of molecule that forms a bond with a nucleophile. Electrophiles can…
Q: D. isoamyl alcohol 38. An aromatic ring should satisfy Huckel's rule, wherein the number of…
A: Aromatic compounds are those which obey Huckel rule and which has 4n + 2 pie electrons.
Q: Write an additional resonance contributing structure for each carbocation and state which of the two…
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Q: Bicyclo[2.2.1]heptan-7-one + PCC (in CH₂Cl₂) => A.) Bicyclo[2.2.1]heptan-7-ol B.)…
A: PCC oxidizes alcohols . From primary alcohols to aldehydes and from secondary alcohols to ketones.…
Q: 5.) Which exhibit both electrophilic aromatic substitution and free radical substitution reaction?…
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Q: Arrange the following alkyl halide in order of increasing E1/ E2reactivity:
A: Elimination reaction occurs either via E1 mechanism or E2 mechanism. E1 mechanism occurs via 2 step…
Q: OH OH OH II III
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Q: True or False: 1. If the reactants are more stable than the products, the reaction will be…
A: If the reactant is more stable then it does not go towards product easily hence the reaction will…
Q: Arrange the ketones in order of increasing reactivity toward nucleophilic addition H3C (I) O(least…
A: Reactivity of ketones towards nucleophilic addition
Q: Alkenes typically undergo electrophilic additions reactions A) True B) False
A: The given statement is - Alkenes typically undergo electrophilic additions reactions.
Q: Provide a detailed, stepwise mechanism for the following transformation. Use the curved arrow…
A: Concentrated H2SO4 act as a source of H+ ion
Q: Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution…
A: Applying concept of ortha para directing group and ring deactivating group.
Q: 4. Identify the position where electrophilic aromatic substitution is most favorable. * HN' CH3 CH3…
A: EWGs are meta directing whereas EDGs are ortho para directing.
Q: 12. Which of the following is aromatic? A) B) HN- C) D) H. ZI
A: A compound is aromatic if it is planar and have 4n+2 electrons in conjugation.
![Rank the following structures in order of decreasing electrophile strength.
most electrophilic
least electrophilic
CF3
`CF3
Н](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F324696c5-32e2-4083-9c11-1b27590914e5%2F16733df7-acc3-401c-8d72-c4144efa2bd4%2F5g5u2pf.png&w=3840&q=75)
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- 12) Use the curved arrow formalism to show the movement of electron pairs in the following reaction and label each reactant as a nucleophile or an electrophile. CHÍNH CHỊCH, + CO Học Nha CH₂CH₂CIProvide a synthetic strategy for the construction of molecule Q from molecule R. You may use any reactants/reagents/conditions that are necessary for your synthesis to be successful. CHO CN &=0 OHC Q RCH3 CH3 CH3 CH;=ĊCH,CHCH;OH H2SO4, H3C H3C Referring to the above reaction: 1. Which atom does the H2SO4 first remove? 2. Identify the reaction if it's hydrogenation, hydrohalogenation, etc. 3. Propose a mechanism for the reaction, using the arrow formalism to indicate the flow of electrons.
- ST03Q3137 Give the major product(s) of the following reaction. fuming H2SO4 (1 mole) heatA certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis gave CH3(CH2), CO₂H and HO₂CCH2CH2CH2CH2CO₂H as the only products. Draw a reasonable structure for this hydrocarbon. Click and drag to start drawing a structure. D:3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOH
- C17T04Q6985 Give the major product(s) of the following reaction. KMN04, H* ? heat on OH OH There is no reaction under these conditions or the correct product is not listed here.K app.101edu.co Lepadiformine is a cytotoxic marine alkaloid that has cardiovascular biological activity. Draw the product of this key SN2 reaction (shown below) used in the synthesis of lepadiformine. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. Br Si e H Draw SN2 product THFRank the following groups in order of priority from highest (1) to lowest (3). < < -COO- -CH3 -NHCH3
- (a) Rank the following carbocations in order of increasing electrophilicity (1 = lowest electrophilicity, 4 = highest electrophilicity). (b) Rank the following 1,1-halomethylcyclopentanes in order of reactivity in an SN1 reaction (1 = lowest reactivity, 4 = highest reactivity. CH3 CI B with SNI, nor reactive means more stable (c) Rank the following species in terms of increasing nucleophilicity in an SN2 reaction in a po aprotic solvent (1 = lowest nucleophilicity, 4 = highest nucleophilicity).Draw the alkene that would react with the reagent given to account for the product formed. ? + + H₂O **** H₂S04 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH3 CHCCH3 | | OH CH3 +12. Explain the selectivity of the following reaction, which produces a single product despite both alkene carbons being equally substituted. H3C CF3 HBr CF3 H3C CF3 H3C Br- H3C only product -H CF3
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