QUESTION 5 Fill in the blanks and follow the directions to complete the 2-step synthesis given below. Use the Reagent Cabinet List to help you answer this question. Answers that require multiple reagents should list reagents in alphabetical order, separated by commas. R groups should be written out in condensed formula Do NOT use superscript or subscripts in your answers. Reaction Reaction Intermediate Starting Material Product Name the functional group found in the starting material and the product. Starting material: Product. Recall your synthesis map. Name the functional group that appears in the Intermediate Product during this synthesis. Intermediate Product Provide the reagent(s) needed for reactions A and B. Assume acidic workups if needed. Reaction A Reaction B:

Q: Question 2 Which of the following is correct for the 15t ionization energies of S, Se, F S>P> Se

A: Ionization energy or Ionization potential : The amount of energy required to remove one electron…

Q: Complete the following table to show what functional groups are present in each of the reagents and…

A: Functional group is the groups or atoms present in the molecule which shows the characteristic…

Q: Following a reaction period of 150-minutes, you decide to perform an extraction to eliminate any…

A: Solvent-solvent extraction:

Q: Convert 2.05×10−3 m2.05×10−3 m to the equivalent length in nanometers.

A: The solution is given below -

Q: 5. Use the following information to answer Question 5. Organic Compound Legend White - hydrogen atom…

A: The given example is an aliphatic compound containing carbonyl group and hydroxyl group.

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A: Nucleophiles are the chemical species which have a pair of electrons to donate. They donate the…

Q: 7) Which statement about chemical equilibrium is not true? A) The same equilibrium state can be…

A: 7) Chemical equilibrium: It is a state where the rate of the forward reaction is equal to the rate…

Q: Draw the product formed in each reaction below. Part 1 of 2 3 H₂C– H₁C CH₂ Pd + H₂ Draw the…

A:

Q: Consider the reaction conditions provided in the question(s) below question. Determine the type of…

A: Alkyl halide gives an elimination reaction by reacting with a strong base. E2 reaction involves a…

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A: The solution is given below -

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A: -> Epoxide ring can be opened with nucleophile and alcohol formed . -> Grignard reagent has…

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A: The structural formula and name of the oxidation products of ethyl alcohol with chromic acid is…

Q: Question 9: Draw the organic products formed in each reaction. a. H-C=C-H [1] NaH [2] (CH3)₂CHCH₂CI…

A: The question is about the reaction of alkyne. We have to draw the final product of the reaction…

Q: 1) Draw a carboxylic acid between 7-9 carbons. Give the IUPAC name. 2) React this carboxylic acid…

A: Carboxylic acid are acid RCOOH where R is alkyl chain

Q: Questions 14-18. Consider each of the esters below when answering the following questions: CO Et…

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

Q: Select the correct product for this reaction Select an answer and submit. For keyboard navigation,…

A: When ketone reacts with grignard reagent followed by hydrolysis gives 3° alcohol.

Q: How would melting point determination help us narrow down the identity of a product or products of…

A: How would melting point determination help us narrow down the identity of a product

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A: Here we have to shift the equilibrium to product side of the reaction i.e dehydration of…

Q: What is the role of the catalyst in electrophilic aromatic substitution reactions of benzene? O A.…

A: The role of the catalyst in electrophilic aromatic substitution reactions of benzene

Q: -24 Each of the following aldehydes is named incorrectly. However, the names give correct structural…

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Q: Why is it important that we are very careful in how much acid is added to neutralize the reaction?…

A: If too much acid is added during crystallization after neutralization value then acid will increase…

Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. H2, Rh/C heat Ⓡ

A: This is hydrogenation reaction. In this reaction benzene ring convert into cyclohexane ring.

Q: 5. Consider the reaction below to answer the following questions: + H₂O HO- a. vicinal diol b.…

A: 5) The base attacks the ketone in the first step and hydrolysis takes place in the second step to…

Q: Question 10: Draw the products formed when CH3CH₂C=C Nat reacts with each a. CH₂CH₂CH₂Br b.…

A:

Q: Please help me figure out the IUPAC names that come from combining the compounds in the first column…

A:

Q: QUESTION 29 What is the mass of the organic fragment of 2-chloro35-3-phenyl-prop-1-yne? O 150 amu O…

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: ccurs, you đó not have to list any tYpe of products..) Test Tube Labeled A) contains: 2-butanol and…

A: Benedict's reagent is a complicated combination of sodium carbonate, sodium citrate, and copper(II)…

Q: What is/are the major product(s) of this dehydration reaction? OH H2SO4 heat А. В. C. D. O A

A: The products of the given dehydration are/is as follows:

Q: QUESTION 5 Predict the product for the following reactions: HO- 1. NaOH 2. CH,CH,Br H2 HBr C. O-CH3…

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: 1. There are three alkene products possible in the dehydration of 3,3-dimethyl- 2-butanol. Draw two…

A:

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.