What product is formed when 1-bromopropane reacts with each of the following nucleophiles? с. СH;S d. HS e. CH3O¯ f. CH;NH2 а. НО b. NH2

Q: Rank the nucleophiles in each group in order of increasing nucleophilicity. а. "ОН, NH, Ha0 b. "OH,…

A: The reagents which have a greater affinity for the positively charged species are known as…

Q: 10. Please show how each compound might be synthesized by the Sx2 displacement of an alkyl halide.…

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Q: Which molecule can loose a hydrogen and become a nucleophile? Select one: a. H3C– ECH b. H;C- -CH3…

A: The terminal alkynes or 1-alkynes are weak acids and loose a hydrogen when treated with strong base…

Q: 2. A. Rank the following compounds by the rate of SN1 reactivity. Molecule that reacts fastest with…

A: The SN1 reaction is a unimolecular nucleophilic substitution reaction. The nucleophile is a chemical…

Q: 46. The Strength of Nucleophile: Which one is the strongest nucleophile? (A) OH (B) -CH3 -CH3 (D)…

A: As we go to down the group, size increases, basicity decreases and Nucleophilicity increases. C…

Q: Rank the following compounds from most to least reactive in an SN1 reaction. عد ماملیه مالیه O T >…

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Q: (f) This part of the question refers to the substituted alcohol (N) given below. CH3 Br N (i)…

A: If the carbon atom directly attached to halogen is further attached to one,two or three carbon…

Q: Which of the following compound(s) may not be converted to a good nucleophile by LDA? OCH3 I II or…

A: Lithium diisopropyl amide (LDA) is bulkier and stronger base. The structure of LDA is  Due to…

Q: Benzyl chloride is reacted with different nucleophiles (HO-, CH3COO-, PhO-, CH3O-). Arrange them in…

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Q: A benzene ring reacts with these reagents in order: 1) Cl2, AlCl3 2) Mg 3) CH3CH2CHO 4) H + 5) conc.…

A: Following reaction occur with the benzene in the order as-

Q: ?Which alkyl halide would be most reactive in an SN1 reaction Br Br Br II II Br Br IV IIIa O VbO I…

A: Given alkyl halides,

Q: What product(s) is/are formed in the following reaction which demonstrates that a S atom is a better…

A: In Organic Chemistry, Heterocyclic compounds are more reactive than benzene because of the greater…

Q: Draw the substitution product that results when CH,CH2CH;CH,Br reacts with each nucleophile. d.…

A: Since you have asked question with multiple part we will only solve 1st three parts. If you want…

Q: Give the minor elimination product(s) of the following compound. ? (CH3)3COK heat Br CH,

A: Base pushes alkyl group to get eliminated and the formation of alkene is favored. In the present…

Q: OH `NH2 OCH3 CI 7. Which would be the least reactive to nucleophiles? 8. Which will react with SOCI2…

A: Acyl derivatives reacts with a variety of nucleophile and because the product cam depend on the…

Q: Rank the attached alkyl halides in order of increasing reactivity in E2elimination. Then do the same…

A: Elimination reaction is a chemical reaction, which involves the removal of atoms in groups or pairs…

Q: When a single compound contains both a nucleophile and a leavinggroup, an intramolecular reaction…

A: When nucleophile substitutes a leaving group, such reactions are called nucleophilic substitution…

Q: (d) O (e) os. (f) os- NH or or (g) (h) or (i) CH3S or CH;Se or NH PH (j) CH3SE Br

A: This is a question with multiple subparts. So, as per bartleby guidelines I need to solve first…

Q: Which of the following is most prone to hydration (acid-catalyzed reaction with water)? a. b. C. d.…

A: Aldehyde which is most prone to hydration is.

Q: In SN2 reactions of haloalkanes, the order of reactivity is RI>RBr>RCl>RF. Alkyl iodides…

A: If the bond is more polarized then it is easy to break the bond and leaving the group, therefore,…

Q: 48. Arrange the following substrates in order of decreasing rates for the dissociative mechanism…

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Q: The following reaction takes place several times faster than the reaction of 2-chlorobutane with…

A: The enhances rate of reaction is due to presence of -N..Et2 which undergoes intro molecular SN2…

Q: Please answer this question

A: Nucleophiles are  the molecules or substances that have tendency to donate electrons or react with…

Q: Which nucleophile would be best for converting a tertiary alkyl halide into an alcohol? CH3O CH3OH O…

A: Answer is explained below. Tertiary alkyl halide can be converted into alcohols via nucleophilic…

Q: Same reaction as in Q1. H3PO4 Identify the nucleophile: H2PO4t- H20 H30* H3PO4 А В D E O A O B O E

A: The nucleophile in the given reaction = ?

Q: Which of the two is the stronger nucleophile? Select one: a CH3OH b. CH3O Which is a polar aprotic…

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Q: Which is the correct order of reactivity towards a nucleophile, from most reactive to least? H3CO F…

A: Given compounds:

Q: Arrange the following ketones in order of increasing reactivity towards nucleophiles with the least…

A: The carbonyl compounds give nucleophilic addition reactions. The carbon atom of the carbonyl carbon…

Q: Which of the following is the STRONGEST nucleophile? -H- -OH I II II IV а. I b. II с. Ш d. IV

A: a) The compound I is the weakest nucleophile because there is no heteroatom as well as it is…

Q: Which member of each pair is a better nucleophile in methanol?

A: “Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: Which of the following is the best (strongest) nucleophile? NH3 H20 NH2 CH30 II II IV Select one:…

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Q: Draw the configuration(s) of the substitution product(s) formed from the reaction of the following…

A: a) Please find below the substitution product for the above reaction  Since the attack will happen…

Q: 10. Alkyl diazonium salts decompose to form carbocations, which go on to form products of…

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Q: (8) Which nucleophile in cach pair will react faster in SN2 reactions? Circle one choice in cach…

A: Nucleophile donates a pair of electrons to bond with the other atom. Molecules or ions with one or…

Q: A crossed Claisen reaction between methylpropanoate and methyl acetate is not synthetically useful…

A: In the case of reaction 1, both of the esters are enolizable. So, the reaction can take place…

Q: 4. For the following, a) predict the product and b) using curved arrows to show electron movement,…

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Q: Rank the following species in each set from best nucleophile to poorest nucleophile.

A: A good nucleophile has a very good tendency to donate electrons.

Q: 9. Rank the following nucleophiles, in a solution of DMF, in order of weakest to strongest. НО CI…

A: DMF is a solvent known as dimethylformamide. It is a polar aprotic solvent. It doesn’t form hydrogen…

Q: 40. Which sacleophile would afford the greatest amount of the substitution product shown below? Br…

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Q: Rank the following compounds in order of increasing reactivity with nucleophiles (from least…

A: In this question, we want to arrange all three Compound in the Increases order of reactivity.  How…

Q: Which reaction(s) would occur in the reaction below (substitution, elimination, both, or neither)?…

A: the correct option is:

Q: 5. Rank the following according to increasing reactivity (1- least reactive, 4 – most reactive in a…

A: The question is based on the concept of organic reactions. We have to identify the reactivity order…

Q: Consider the following reaction: H₂O: CI OH What is the rate-determining step in this reaction?…

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Q: The following Friedel-Crafts Alkylation reaction usually results from the disubstituted product from…

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Q: X H₂O - g E2 Elimination h = SM1 Nucleophilic subst

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Q: In the reaction CH4 + C12 --> CH3CI + HCI, which is the nucleophile? A) CH4 B) C12 C) HCI D CH3CI E…

A: Given- CH4+Cl2-->> CH3Cl + HCl

Q: *NH OCH CI 7. Which would be the least reactive to nucleophiles? 8. Which will react with SOCI2 to…

A: A question based on Nucleophilic substitution reaction, which is to be accomplished.

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.