How would this synthesis go? The image depicts a chemical reaction equation. - **Reactants:** - The first compound is bromoethane, represented as a two-carbon chain with a bromine (Br) atom attached to the second carbon. - The second compound is sodium ethoxide, shown as a two-carbon chain with an oxygen (O) atom bonded to sodium (Na).- **Products:** - The product is ethyl alcohol (ethanol), displayed as a two-carbon chain with an attached hydroxyl group (OH).- **Reaction Details:** - The reaction involves the substitution of the bromine atom in bromoethane with the ethoxide ion from sodium ethoxide, resulting in the formation of ethanol. This equation represents a nucleophilic substitution reaction where the ethoxide ion acts as the nucleophile, displacing the bromine atom in bromoethane.

Alkyl bromide reacts with an alcohol (sodium alkoxide) to form an ether by the Williamson ether…

Answered: How would this synthesis go?

Science

Chemistry

How would this synthesis go?

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Related questions

Q: 21. During decarboxylation, which final step occurs after carbon dioxide has been lost? a. keto-enol…

A: In decarboxylation reaction, CO2 gets eliminated and we get ketone as a final product. In aldol…

Q: Show how to carry out the synthesis below. Br HO

Q: `OH CI

A: See products in red boxes.

Q: i-step synthetic pathway below by filling in the missing products along Synthesis B Synthesis C…

Q: The rate constant for the uncatalyzed reaction of two molecules of glycine ethyl ester to form…

Q: synthesis of this starting from cyclohexanone. I was thinking oh adding benzene, ethylene, and…

A: Here clearly mentioned that you have to start it from cyclohexane. Lets start it step by step…

Q: Name the following compound KOH

Q: Show how you might synthesize ethynyl benzene from methyl phenyl ketone.

A: When methyl phenyl ketone is treated with Zinc and mercury in presence of the concentrated…

Q: Steroids are a class of organic compounds containing a specific tetracyclic skeleton (four rings),…

A: Given : We have to draw second step for the given reaction.

Q: What would be the Hnmr of the following compound? :0

A: The 1H NMR spectrum of 1-(2-methoxyphenyl)ethan-1-one would show signals corresponding to the…

Q: Predict the product of the following 5-step reaction. Based on the product, identify which alkene…

Q: он NaOH

A: On reaction with NaOH, below geven compound is formed :

Q: Show by equations how you would convert ethyl acetate to: (a) acetic acid; (b) ethanol; (c) t-butyl…

Q: Complete the synthesis of the target molecules below (on the left) from the starting material (on…

Q: show the mechanism for the reaction

A: The reactions involving organic compound are called organic reactions. Reaction mechanism gives the…

Q: ОН B) 'N. H

Q: iii. only O i. only none of the other answer choices are correct O iv. only ii. only

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts. 4…

Q: Propose a method on how you will synthesize 5-methyl-4-octanal from 4-methyl-4-octene

A: A reaction can proceed in the forward direction if it attains the minimum required energy…

Q: 1) SOCрyridine 2) CH3O- d) 1) TsC/pyridine 2) CH30 e) "OH HBr f) "OH

A: d) Reaction of alcohol with SOCl2 in pyridine produces, alkyl halide. OH group is replaced by Cl…

Q: Q₁1 Prepare avinyl chloride From Acetylene cl

A: To solve this problem we have to complete the given chemical reaction.

Q: Synthesis the following. H₂N HOON

A: The question is based on the concept of organic synthesis. we need to synthesize the product using…

Q: Which of the following reactions will NOT produce a carboxylic acid? CN 0 Question 50 Listen NH₂ CN…

A: Given are organic reactions. We can get carboxylic acid from various compounds such as alcohols ,…

Q: CH3 benzene +CH,CI– AICI, toluene

Q: h) i) j) type +Br Br type OH Selective Catalytic Hydrogenation o-Nato CO₂H type EtOH OEt a) SOCI2, D…

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: Predict the major organic product of the given reaction and complete its mechanism. 1. NaOEt/EtOH 2.…

A: Step 1: Acetoacetic ester with sodium ethoxide and ethanol deprotonates the acidic proton and forms…

Q: QUESTION 5 Show how you would synthesis the following compounds starting from benzene? Write the…

A: We have to synthesise the given compound starting from Benzene. We have to make use of different…

Q: Find out the order of following reaction: 2NO₂ → 2N0 +0₂ H₂+1₁₂→ 2HI - H2C12 (hv) → HCL C12H22011 +…

A: ( If you have any questions related to this problem please feel free to ask me).

Q: 1. Which of the following reactions will not occur? A) CH3CH=CH₂Br + (CH3CH₂)2Culi → B) CH3CH₂Br +…

Q: H 100 Br H ** CH3 NH₂

A: Given that, a synthesis scheme is shown below We have to carry out the above synthesis in two…

Q: As written, the following synthesis scheme is flawed. Draw the actual product(s) that would be…

A: An organic compound can be converted into another compound using different reagents. Reagents are…

Q: Determine the intermediates and product(s) for the following synthesis sequence. O d ملی میں LDA HD…

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: Can you please draw me the synthetic route (not mechanisms) for this reaction by using…

A: Step I : conjugate addition of OH to unsaturated ketone. Step II : it is an haloform reaction in…

Q: Which of the following is an effective way to complete the synthes below. O LNH, 2) H₂O* 1) HNOyH₂50…

Q: Which of the following is correct? OH NH4NO3 There is no example based on reduction mechanism in the…

A: The initial reactant is benzaldehyde.It then form benzoin with the structure shown below:This…

Q: Draw the structure of the organic product that is formed when the compound shown below is treated…

A: Given that, the reaction is:

Q: 22. Using propene and bromo-ethane as the only sources of carbon and using any reaction conditions…

A: Answer:- This question is answered by using the simple concept of chemical reactions of organic…

Q: None

A: Step 1:First step (top left): The starting material is cyclopentene. To convert this to a…

Q: Perform the following retrosynthesis. OH NO2 NO, он Он

A: The answer for first question is given below. Kindly repost the other question as separate one.

Q: O Complete the following: Stereochemistry and regiochemistry may be important. a) téo,c" C) d) type…

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: 4. Terpenes are substances derived from active isoprene or isopropyl pyrophosphate, they are the…

Question

How would this synthesis go?

The image depicts a chemical reaction equation.

- **Reactants:**
- The first compound is bromoethane, represented as a two-carbon chain with a bromine (Br) atom attached to the second carbon.
- The second compound is sodium ethoxide, shown as a two-carbon chain with an oxygen (O) atom bonded to sodium (Na).

- **Products:**
- The product is ethyl alcohol (ethanol), displayed as a two-carbon chain with an attached hydroxyl group (OH).

- **Reaction Details:**
- The reaction involves the substitution of the bromine atom in bromoethane with the ethoxide ion from sodium ethoxide, resulting in the formation of ethanol.

This equation represents a nucleophilic substitution reaction where the ethoxide ion acts as the nucleophile, displacing the bromine atom in bromoethane.

Expert Solution

This question has been solved!

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

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 1 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

i) How could you synthesize dipropyl ether from propan-1-ol, TcCl and any other inorganic reagents? Draw the synthetic scheme (likely 2-3 steps) ii) Draw what organic side product might you see from this reaction?
Complete the following reaction and propose a mechanism
Provide a detailed mechanism for the following reactions. H₂SO4 CI 1.NaOH, Heat, pressure 2. HC1, H₂O CH₂ LOH CH₂ H₂O OH
Show how you would make the target molecule from the provided starting structure. Show all intermediate structures, do not show any mechanisms. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. To preview the image click here CI O₂N. CO₂H
answer asap, thank you
Please send me answer of this question within 10 min i will give you like sure.sende typed answer only please
(a) In an acid-catalyzed hydration, one of the following 10 carbon alkynes is expected to produce a single hydration product? Select the correct alkyne and draw the structure of the hydration product that is formed from this alkyne. (I) 2-decyne; (II) 3-decyne; (III) 4-decyne; (IV) 5-decyne; (V) none of these will give a single hydration product. (b) The reaction shown below gives Compound X as the major product. The mass spectrum of X is shown. Br2, H20 Compound X 100 - MS-IW-5644 80 60 40 - 20 - 20 40 60 80 100 120 140 160 180 200 220 m/z Considering the reactions of alkynes and the MS data, de duce which of following structures corresponds to X: Br Br HO, IV V I II II Support your answer with a reaction mechanism for fomation of X and identification of relevant peaks in the mass spectrum. 12 Relative Intensity
Give the main organic product that would form after the following reaction steps. 1) HO 2) HBr 3) Mg OH, 4) CO₂ 5) H3O+/A H* Gee die hooforganiese produk wat sou vorm na die volgende reaksie stappe.
3. Propose a synthesis for each product from the respective reactant, which goes by way of a benzyne intermediate. If the specified product is the only product which is formed, indicate that. If the specified product is not the only product formed, draw the structure(s) of any other isomers formed (but choose a route which forms only the desired product, if possible). CF3 НО CF3 H,N CH3 CH3 CH3
Which of the methods shown will successfully complete the following synthesis? OH NH 1) 1) PBR3 3) 1) H2CRO4 2). NH2 HO, 2) SOCI2 NH2 3) 2 3) aqueous NaOH 1) H2CRO4 1) PCC, CH2CI2 2) 2) SOCI2 4) HO 3) 2 NH2 OH 2) NH2 H+ 4) LIAIH4 ether followed by H2O O 1 O 2
starting from acetylene as the only carbon-containing chemical, along with any other chemicals show the mechanism of how to synthesize 1-propanol.