Select the major organic product resulting from the sequence of the reactions written.CH3Zn(Hg)HCIAICI3CH3CH,CH2CH,CH,CH,CH3CH,CH,CH,CH;CH,CH3CH(CH3)224.0 1O 2O 3Moving +

Answered: Image /qna-images/answer/18cd5c0e-5e64-4f75-8b3a-baadd4c5bd6f.jpg

Answered: Select the major organic product…

Select the major organic product resulting from the sequence of the reactions written. CH3 Zn(Hg) AICI3 HCI CH, CH3 CH,CH2C H,CH, CH3 CH CH,CH CH-CH,CH; CH(CH3)2 2 4 0 1 O 2 O 3

Pushing Electrons

4th Edition

ISBN:9781133951889

Author:Weeks, Daniel P.

Publisher:Weeks, Daniel P.

Chapter3: Mechanisms

Section: Chapter Questions

Problem 93EQ

See similar textbooks

Related questions

Q: CH3CH2OH PCI3 or SOCI2 F G |CH3OH / H* 1. NaBH4 M 2. Но N t2-CHz-C-OH

A: Given

Q: Which of the following statements correctly describe(s) E2 reactions of alkyl halides (RX)? III.…

Q: 1. NaOH Nal H OH OH 2. H3PO4 H20 Meo 80° Meo f = Syl Nucleophilic substitution g = Sy2 Nucleophilic…

A: Reaction 1 - These reaction proceed by SN2 reaction mechanism because in product complete inversion…

Q: Starting with benzene, which set of reagents A through D will yield the product? Click on a letter A…

A: To get ortho product we should have introduce a ortho directing group here it is acyl group which…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. 1. lithium…

A: Given starting material is ketone.

Q: 4 pts Provide the structure of the major organic product. in the following reaction sequence. 1.…

A: Answer:- This question is answered by using the simple concept of chemical reaction of ketone with…

Q: Pd(OAc)9, 2 PhgP 2 C,H;CH=CH, + I- I (CH3CH2) §N

Q: 3. Predict the product involving the carbylamine reaction. Indicate NR if there is NO REACTION. а.…

A: There are two reaction asked in question , we have to predict whether the product will form or not…

Q: CH;CH, + :Ci–ĞI: ight CH,CH,-Ci: H-Cl: + A. Provide the chain-initiating and chain-propagating steps…

Q: Br, NH, NH, CH,Br H2, Pd (а) (b) CH3 H.

Q: Select the reagents for the following transformation. Please enter your answer as a string of…

A: Detail mechanistic pathway is given below to find out the necessary reagents to accomplish the…

Q: In each case below select the synthetic procedure that could be used to carry out the transform The…

A: A question based on addition to alkene, which is to be accomplished.

Q: 1. H2CrO4 2. SOCI2, pyr. 3. (CH,CH2)2NH (xs) HO-

A: The reaction given is,

Q: b) Complete the following reactions of alkenes and alkynes by providing the structures of the…

A: ii) Alkynes react with Br2 molecules and form dibromo alkene first which again reacts with Br2 and…

Q: Which alcohol is formed from the acid-catalyzed hydration of the following alkene? H CH3 H,0 H2SO4…

Q: 4. Write the following sequence of reactions: HNO3 conc. A H2SO4 conc. CH;CI В AICI3 Cact, t°C 3…

Q: Show the synthesis of the target molecule from the starting material, and explain how you got the…

A: The organic reaction is carried out in many steps. To perform every step, reagents are needed. When…

Q: 3. Write the product and the mechanism for reaction: Kynol. to H3C H₂C AICI3

Q: :0: || CH-C-CI: :0: CH-SH CH-C-S CH. +

Q: 2. State the reaction happening in each step of the synthesis sequence shown below. H2C=CH, CH;CH2OH…

A: Solution : Dehydration reaction involves the loss of water molecules. This reaction is mainly…

Q: What is the organic product formed in the following sequence of reactions? Br (1) Mg/ether, (2) CO₂…

A: The three step synthesis is shown in the following step.

Q: Complete the following reactions by providing the missing products and reagents A-G. i) OH H₂PO4…

A: Alkene in presence of m-CPBA undergo epoxidation reaction. This is one type of oxidation reaction.…

Q: 6. Draw the structure for compound A and for compound B in the following synthetic sequence. 1) Mg.…

A: In this question we have to tell the product of the reaction.

Q: I: Predict the products of the ff: substitution reactions and show the mechanisms involve. (a)…

A: In presence of polar aprotic solvent , nucleophilic Substitution type 2 takes place . For SN2…

Q: но. H,SO4 + H,0 `OH Acetic Acid Isoamyl/Isopentyl Alcohol Isoamyl/Isopentyl Acetate

A: In the Fischer Esterification reaction, a carboxylic acid and an alcohol react to form an ester.

Q: The following reaction schemes have flaws as presented. Which of the following statement is the best…

A: Option D is correct answer.

Q: Which of the following methods would give the product? H=H НО. A. 1. NaNH₂ 2. CH₂=CHCH₂Br 3.…

Q: OH 1. aqueous H2SO4 CH3 CH3 2. H2SO4 OH H2O 130° a = Proton transfer d = El Elimination f= SN1…

A: Hydration of alkene: Alkene gives hydration reactions in presence of an acid catalyst. In this…

Q: Which compound would be the product of the reaction sequence shown below? MgBr 2. H30*/H20 3. РСС 4.…

A: RMgBr is a grignard reagent and it attacks the carbon attached to double bonded Oxygen atom and join…

Q: The following can undergo 1,2- or 1,4-addition reactions. Predict the major organic product from…

A: In a functional group same type of reagent reacts, and forming different type of products. This is…

Q: What is the final organic product of the reaction sequence shown? 1) CH3O Na+ 2) CH2=CHCH,Br 3) CH,O…

A: Given starting compound is methyl acetoacetate. In the given reaction there are two alkylation take…

Q: 4. Give the products of the following reactions. CH₂ (i) KMnO₂. OH, A a.) (ii) H₂O* b.) CH3COOH +…

A: Given reactions are : Give the products of the following reactions = ?

Q: b) Complete the following reactions of alkenes and alkynes by providing the structures of the…

A: Since you have posted question with multiple sub-parts, we are entitled to answer the first 3 only.

Q: 5) Give products (major and rearranged) and mechanisms for the follwing. CH3 HBr ČH2CH3 a) + NaOH…

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

Q: 4. Give the products of the following reactions. C CH3 (i) KMnO, OH, A (ii) H₂O* CH3COOH + PC13…

A: Here we are required to predict the product of the reaction

Q: 7. Complete the following reactions of alkenes and alkynes by providing the structures of the…

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Draw a structural formula for the major organic product of each reaction and specify the most likely…

A: To determine the mechanism to which the product is formed as,

Q: 18) C,H,OK" Write all the elemination and substitution products 19) H;CO, 20) KMnO,

A: "Since, you have posted multiple question, we will solve only first 3 for you, to get other question…

Q: Give the products of the following reactions. CH3 (i) KMnO4, OH, A (ii) H₂O* CH3COOH + PC13 BrCH₂CH3…

A: Here we are required to find the product of the reaction

Q: 1. Give the major organic product (s) for the following reactions or sequence of reactions. 1)…

Q: 4. Determine the structure of compoundsD-F in the following reaction sequence. 1. NaH NABH4 1. NaH F…

Q: Write the mechanism and predict the most likely product in the following reaction NaOH ICH2CH3…

Q: Aniline can be synthesized from benzene by using correct synthetic schemes. Choose one scheme that…

A: Please find your solution below : For converting benzene to aniline, first benzene is converted to…

Q: CH3 CH3 H.c--CH; 1. H20 H3C- H3C ČH3 2. NaOH HBr H20 Br a = Proton transfer d = El Elimination f=…

A: To solve this problem we need to write the mechanism of the given reactions.

Q: CH3 H3C OH Br2 H20 CH3 CH3 H3C H3C Br Electrophilic addition of hypohalous acids to alkenes yields a…

Q: The following reaction schemes have flaws as presented. Which of the following statement is the best…

A: Given scheme is an example of electrophilic substitution reaction. In this reaction, Friedel craft…

Q: NMe, HO, CH3 H3C CI N(CH2CH3)3 Dimethylaminopyridine (DMAP) is often used as a catalyst in…

Q: What is the major organic product obtained from the following sequence of reactions? 1. NaOCH,CH3…

A: Applying concept of organic synthesis of organic molecules.

Q: OH. " H₂O + CO₂. Nal CH₂ 2. + H₂C-C-CH₂ H₂O a Proton transfer d E1 Elimination = f = SN1…

Concept explainers

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.

Question

100%

Select the major organic product resulting from the sequence of the reactions written.
CH3
Zn(Hg)
HCI
AICI3
CH3
CH,CH2C
H,CH,
CH,
CH3
CH,CH,CH,
CH;CH,CH3
CH(CH3)2
2
4.
0 1
O 2
O 3
Moving +

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

E 21 write mechanisms for the given reactions
(CH3)3CHOH is reacted with CH3-O-C--C6H5 in a transesterification reaction. What is the M+ of the product? || O 102 80 178 None of these
What is the rate law implied by the mechanism given below? CH3COCH3(aq) + H+(aq) ←→ CH3C(OH)CH3+(aq) (fast, reversible) CH3C(OH)CH3+(aq) → CH3C(OH)=CH2(aq) + H+(aq) (slow) CH3C(OH)=CH2(aq) + Br2(aq) → CH3C(OH)CH2Br+(aq) + Br-(aq) (fast) CH3C(OH)CH2Br+(aq) → CH3COCH2Br(aq) + H+(aq) (fast) A. Rate = k[CH3COCH3][H+] B. Rate = k[CH3COCH3] C. Rate = k[CH3COCH3][Br2] D. Rate = k[CH3COCH3]2 E. Rate = k[CH3COCH3][Br2]/[H+] (Answer is A, looking for explanation why!).
a. Propose a synthetic pathway for cis-[NiCl2(CO)2] using trans-effect. b. Propose the methods to differentiate the isomers in between [RhCl2(H2O)4]Cl and [RhCl3(H2O)3].H2O.
I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.
The rate constant for the uncatalyzed reaction of two molecules of glycine ethyl ester to form glycylglycine ethyl ester is 0.6 M- 1s - 1. In the presence of Co2 +, the rate constant is 1.5 * 106 M- 1s - 1. What rate enhancement does the catalyst provide?
Qa 18. Bromination of 5a-cholestan-3-one occurs at C-2 or C-4 to give 2 regioisomers. Two unsaturated ketones with lambdamax = 230 nm and lambdamax = 241 nm are yielded during dehydrobromination. Use Woodward-Fieser rules to distinguish between the two.
The BOD rate constant was found to be 0.151 day^-1 (base e) at 28.5 Celsius. What is the rate constant day^-1 (base e) at 6.0 Celsius?
Draw reaction mechanism for week 2 A wittig reaction experiment: Week 1 -》 preparation of phosphonium salt Materials : triphenylphosphine (5.3g),methyl Bromoacetate 3.36g (2.1ml) , ethanol 30ml . The yield obtained was 8.93g .The percentage yield was 106.4% Week 2 -》 Formation of the ylide and wittig reaction Materials :Phosphonium salt (5g), napthyl-2- carboxaldehyde( 2.65g), 20 ml of water and 5 nl of Nahco3. Yield obtained was 0.51g . The percentage yield was 14.2%. Week 3: Solvent free wittig reaction Materials: Benzyltriphenylphosphonium chloride (0.5g ), 4 - Bromoabenzaldehyde (0.24g), Potassium phosphate (tribasi c) 0.275g .The yield obtained was 1.21g. The percentage yield was 35.6%.
Fill in the blank: The acid catalyzed hydration of alkenes (addition of H2O/H2SO4) is: A) a polar mechanism with carbocation intermediate B) a radical mechanism with carbon radical intermediate C) a concerted reaction
CHOOSE THE LETTER OF THE CORRECT ANSWER. What is the major product in the reaction mechanism? reaction mechanisms of organic molecules (alcohol to carboxylic acid) a. But-1-ene b. But-2-ene c. Buta-1,3,-diene d. Butane
________ is reduced in the following reaction: Cr2O72- + 6S2O32- + 14H+ → 2Cr3+ + 3S4O62 + 7H2O O2- S4O62- Cr6+ H+ S2+