7. Identify the nucleophile and leaving group and draw the products of each reaction. -OCH,CH3 C. - a. Br Br .CI NaCN owol of nialqxa (e) NaOH Wood ort aoes Seq nrgilosle bsoubo d. b.

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: Consider the attached E2 reaction Draw the by-products of the reaction and use curved arrows to…

A: Given:

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: Label the reactive features of each molecule and then circle the nucleophile used in the reaction…

A:

Q: e starting materials and reaction conditions suitable for lowing compounds by a procedure involving…

A: As per guidelines first 3 are allowed to answer , please post seperately rest of the subparts to…

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

A:

Q: a good leaving group such as iodide. .CO₂H base НО 15 17 co Mecarmis SN2 ميكا تكيه ها التفاعل + TM3…

A:

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

A: The explantion for the classification stated above is as follows :

Q: a. which reaction is faster ? b. Complete the enerqy diagram c. labei the diagram by drawing the…

A:

Q: Draw the products (including stereochemistry) for attached reaction.

A: Please find below the reaction along with the stereochemistry. Since the attack is possible from…

Q: SN1 solvolysis of t‑butyl chloride, rank the solvents from fastest reaction to slowest reaction.

A:

Q: Vhich is the better nucleophile in protic solvent? or O CI-

A: Solvent which gives hydrogen ions in solution called as polar protic solvent whereas solvent which…

Q: Which halide in the attached marine natural product reacts fastest in the SN1 reaction?

A: Sn1 reaction depends on the stability of carbocation.

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: The product in the first reaction is a ? H,SO, of R =R H20

A: The product of a first reaction has to be identified below.

Q: 3. Rank the following in order by the rate in which they could participate in an SN1 reaction (“1"…

A:

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

A: From among the two benzylic halide given we can tell that the halide A reacts much faster than…

Q: Br "OCH,CH3

A: Reaction of alkyl halides with nucleophile is termed as nucleophilic substitution. It is competed by…

Q: Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products…

A:

Q: Drawing Substitution and Elimination Products from a 2° Alkyl Halide. Explain how ?

A: 2° alkyl halide are defined as alkyl halide in which the carbon atom next to halogen has two carbon…

Q: The quality of the substituent for the elimination reaction is the leaving group ability of it. Like…

A: The best leaving group has to be identified.

Q: This reaction is an example of conjugate addition of a nucleophile to an a.B-unsaturated carbonyl.…

A: conjugate 1,4 addition is called Michael addition

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

A: The primary amines react with NaNO2 and HCl in order to form an alkyl diazonium salt which on…

Q: Fill in the blanks: Good nucleophiles are usually strong mechanism. nucleophiles and a alkyl halide…

A: A nucleophile is defined as a chemical substance that has lone pair of electron or negative charge…

Q: Draw the product of this reaction. Ignore inorganic byproducts. 1. NANH2 2. CH3CH2CH2BR Atoms, Bonds…

A: NaNH2 is basic enough to take alkyne proton. First reaction is acid base reaction then a…

Q: HBr can be added to an alkene in the presence of peroxides (ROOR). What function does the peroxide…

A:

Q: а) b) c) OEt

A: When aldehyde or ketone react with diol or alcohol it form acetal.

Q: The quality of the substituent for the elimination reaction is the leaving group ability of it. Like…

A: In elimination reaction atom/ group of atoms that leave the substrate is called leaving group. Speed…

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

A:

Q: .CI .CI OH2

A: SN2 (substitution nucleophilic) reactions are bimolecular reactions. The rate of SN2 reactions…

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: white reagents for each. - ∙Br OH шон

A: The first reaction is an example of halogenation of an alkyl halide whereas the second reaction is…

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: Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution,…

A:

Q: the reagents are LiAlH4 Et2O / H2O, can you please redo with these reagents? Thank you.

A: We have to give the product of the reaction when methyl benzoate reacts with LiAlH4, Et2O/ H2O.

Q: Rank the alkyl halides in attached group in order of increasing reactivity in an E2 reaction ?

A: E2 elimination reactions follows single step mechanism. The mechanism involves the cleavage of C-H…

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: 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: Can you match best nucleophile / conditions from the list that will give a successful hydrolysis…

A: The best nucleophile/condition that will give a successful hydrolysis reaction for all the…

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: What nucleophile is needed to convert (CH3)2CHCH2CH2Br to each product?

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Organic Chemistry Maxwell presented by Macmillan Learning a) Select the best set of reagents for the…

A:

Q: 1. What is the nucleophile in the reaction? 2. The reaction above follows what mechanism? 3. What is…

A: It is the basic part of the reaction mechanism.  Here we have to be clear about the nucleophile,…

Q: Give the mechanism given bleow reactions with curved arrow and all format harges ? 1-ct y

A:

Q: Part 1 out of 2 Draw the organic product of the reaction. on + -OCH(CH3)2

A: the given reaction is of type is SN2 reaction which is an the addition of the nucleophile and the…

Q: Rank the nucleophiles in each group in order of increasing nucleophilicity.a. -OH, -NH2, H2Ob. -OH,…

A: Nucleophilicity increases with increase in basicity of species.  Across a period from right to left…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.