which compound is the halogen substituted most rapidly by aq hydroxide ions? a. CH3CH2CH2CH2Cl b. (CH3)3CI c. (CH3)3CCl d. CH3CH2CH2CH2I

Q: What is the major product generally formed when a tertiary alkyl bromide  (R3Br) reacts with sodium…

A: the solution are as follows:

Q: Which one of the following is the best(faster reaction) nucleophile for the 2-bromobutane SN1…

A: the strength of nucleophile does not affect the reaction rate of SN1 because the nucleophile is not…

Q: What reagents would you use to carry out the following reaction? (A) H₂ / Pt (B) (C) (D)…

A:

Q: REF: 21.5 A What is the product of the following reaction sequence? CH3 1. TSCI 2. (CH3);ONa ? OH (d…

A: Step I : Conversion of OH group into leaving group OTs using TsCl.  Step II : using base NaO(CH3)3…

Q: Explain the observed rate of reactivity of the following 2° alkyl halides in an SN1 reaction.

A: In SN1 if Cl- leaves the right most compound will form an Aromatic compund with 6e- which is stable.…

Q: Which compound in each pair reacts faster in nucleophilic substitution? a. CH;CH2CH2CI or CH;CH2CH2I…

A: Given pairs, a. CH3CH2CH2Cl  or  CH3CH2CH2I b. (CH3)3CBr  or  (CH3)3CI c. (CH3)3COH  or  (CH3)3COH2+…

Q: Draw the product formed by treating each compound with excess CH3I, followed by Ag2O, and then heat.

A: The complete reaction for a is shown below.

Q: B. Which SN1 reaction of each pair would you expect to take place more rapidly? Explain your answer.…

A: SN1 reaction is the unimolecular nucleophilic substitution reaction in which the nucleophile…

Q: C. CH;OH Is this reaction E1 or E2? elimination product(s) d. NaOH Is this reaction SN1 or SN2?…

A:

Q: Draw the product formed by treating each compound with excess CH3I, followed by Ag2O, and then heat.

A: Hoffmann elimination It is a type of elimination reaction of an alkene where least stable alkene…

Q: e the best reagents to complete the reaction shown below. NaH A (CH3)2CHCH2CI OH NaH B (CH3)2CHCH2F…

A:

Q: Which SN2 reaction is each pair is faster? А. Br H20 Br HO, OH Br Br OCH3 Oc .CI HO, B.

A: In a SN 2 reaction, the nucleophile attacks the alkyl halide from backside, and the bond breaking…

Q: Which synthetic route is the best way to prepare ethyl isopropyl ether? O (CH3)2CHONa + CH3CH2Br O…

A: Ether can be prepared using williamson ether synthesis process. In which primary halide reacts with…

Q: (a) Which is a stronger acid NH2 NH, b. If nitration is done on both the compounds what will be the…

A:

Q: Which benzylic halide reacts faster in an SN1 reaction? Explain.

A: SN1 reaction are reaction in which carbocation formation occur which is rate determining step .…

Q: 8. From the given starting material provide a reasonable synthetic route to the following molecule.…

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Q: Fill in the blanks: B A OH Compound A can be converted to cyclobutanol using the reagent Compound B…

A:

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: Draw the product formed by treating each compound with excess CH3I, followed by Ag,0, and then heat.…

A: Hofmann elimination is a reaction in which amines are eliminated from the molecule to form alkenes.…

Q: 27(c) Most basic nitrogen A or B? (Hint: The lone pairs on the two play different roles in the…

A: The basicity of the nitrogen depends on the availability of electron density on the nitrogen atom in…

Q: Which alkyl halide will react the fastest in an SN2 reaction (CH3)3CI CH3CH2Br CH3CH2I CH3I CH3Br

A: The SN2 reactions is used to denote bimolecular nucleophilic substitution. In this mechanism, a…

Q: which of the following SN2 reactions will be faster? (1) Reactions of CN- (cynaide ion) with…

A: We have to choose for following given SN2 reactions will be faster. (1) Reactions of CN- (cynaide…

Q: SN2 reaction

A:

Q: What is predominant reaction type between 2- bromopentane with sodium ethoxide? O SN1 SN2 O E2 E1

A: 2-bromo pentane with sodium ethoxide  Reaction predominant type is ...

Q: CH3CH2CH2C=CH CH3CH2CH2CHO Reagents a Br2 CH2l2 / Zn(Cu) / ether e 1. O3 2. Zn / H3o* b CH3I H2 /…

A:

Q: Which of the following reactions describes why Acetic Anhyhdride needs to stay dry in order for it…

A: The acetic anhydride is need to stay dry because acetic anhydride in the presence of water gets…

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: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr Br Part 1:…

A: The given reaction is an example of the reaction of secondary alcohol with HBr. Generally, alcohol…

Q: HO ?? TSCI NaOH starting materials EtzN H20, heat IZ

A: This is a Beckmann type rearrangement.

Q: ELOH/H20 NH3 A C D

A:

Q: QVI: Starting from benzene as the only organic reagent you have and use any other inorganic reagents…

A: One mole of Benzene is treated with two moles of nitrating mixture to give 1,3diitrobenzene.…

Q: Which halide is most reactive in SN2 reactions? Select one: -CH2CH2CI ÇI CI H3C ÇI CI CH3

A: Nucleophilic substitution biomolecular reaction (SN2):The bimolecular nucleophilic substitution…

Q: The mechanism by which the haloform reaction works. Explain.

A: We have to give the mechanism of haloform reaction.

Q: A key step in the synthesis of β-vetivone, a major constituent of vetiver, a perennial grass found…

A: LDA acts as a bulky base. It abstracts the ‘H’ from the less hindered site. Step wise mechanism for…

Q: NH2 NH OH d. CH3CH=CHCH3 Reagents Available 1. PB13 2. Mg, ether 3. РСС CH2=CHCH=CH2 8. NANH2 9.…

A: The required reagents for the given conversion are as follows:

Q: Rank the alkyl halides in each group in order of increasing reactivity in an E2 reaction.

A: E2 type of reaction is second order elimination reaction in which the rate of reaction depends on…

Q: hy is bromination more selective than chlorination?

A: bromination more selective than chlorination because

Q: Butanal 1-Butanol Waste: G704 (Non-halogenated organic solvents) 1. NABH, ethanol a.)…

A:

Q: What reagent would you use to do this reaction? H2N HO. O a) HgSO4, H3o* b) KMNO4 O c) Cro3 d)…

A: KMnO4 strong oxidizing agent it cam oxidize almost all compounda even alkyl groupa to carbozylic…

Q: Reagents 2 equivalents of Na H2, Lindlar's catalys Na / NH3 H2SO4, H9SO4 (sia)½BH then H2O2. 1…

A: An organic reaction is carried by some reagents which could introduce desired changes in the…

Q: The SN2 reaction can be best carried out with   A. Primary alkyl halide B. Secondary alkyl halide…

A: The SN2 reaction can be best carried out with --

Q: A Grignard reagent can be produced by combining an alkyl bromide or alkyl chloride with.. A. LICI O…

A: General formula of Grignard reagent is RMgX where  R = alkyl group  Mg = magnesium  X = halogens

Q: Reagents 1. NaOH / H2O 2. H3O* SOCI2 i 1. NABH4 2. H3O* 1. ВНз / THF 2. H2O2 / NaOH f 1. LIAIH, 2.…

A: The organic reactions takes place by adding various reagents, to get the desired final product.

Q: Br 1. Pd°Ln, EtN, MECN, Me Me 2. MCPBA, CH2Cl2 3. HCIO, EIOH provide step by step analysis for each…

A: 1. a. Heck coupling. Epoxidation. Acid catalyzed epoxide opening with ethanol. (epoxide is opened at…

Q: 56. Rate of SN2 reaction: I. CH;CH2CH2CH2CH2BR + CH30/H2O→ II. CH;CH2CH2CH2CH2BR + CH3O°/DMSO→

A: We know that   SN2  reaction is second order reaction because it involves the nucleophile and the…

Q: Reagents 2 equivalents of NaNH2 H2, Lindlar's catalyst Na / NH3 a. HBr m. HBr, H2O2, hv c. H2O,…

A: We have to identify the reagents nessato accomplish the following given reaction as follows in step…

Q: Explain how the reaction of (CH3)2CHCH(Cl)CH3 with H2O yields two substitution products,…

A: This reaction proceeds via SN1 mechanism. The following are the steps: The Cl leaves as Cl-, forming…

Q: Which of the following SN2 reactions occur faster and why? a CH3 H2 -C-Br CH;CH,CHBr + OH or H,C-…

A:

Q: Which are the best reagents for the rxn ċ- CH3 First Step CH2 - N Second Step `CH2CH3 Third Step a.…

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

Q: Rank the alkyl halides in each group in order of increasing reactivity in an E2 reaction.

A: Increasing order of reactivity in E2 mechanism:   a.