a. Br b. ČI c. Br

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: Introduction: Aldol condensation reaction: An Aldol reaction is a type of condensation reaction in…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: The above given reaction for the formation of Benzyl bromide using Toluene. It is based on free…

Q: 9. Identify all functiona l groups (excluding alkanes) for the given molecule (S) b.count all…

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

Q: Identify the most stable carbocation. Select one: О . ОН

A: We have given the organic compound having alcohol as functional group we have to identify the most…

Q: ? Modify the structure of the starting material to draw the major organic product. Use the single…

A:

Q: Which alkyl halides can be prepared in good yield by radical halogenation of an alkane?

A: Alkanes undergo both bromination and chlorination. But Chlorination happens faster than bromination…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: The conversion of starting molecule to desired product takes place in two steps. In step 1 the given…

Q: Draw a second resonance structure for each carbocation. Then draw the hybrid.

A: In the below steps , please find the Resonating structure & hybrid

Q: Which alkene reacts faster with HBr? Explain your choice.

A: When alkene reacts with HBr first we got a carbocation then nucleophile (Br-) attacks to get the…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: A condensation reaction between two aldehyde or ketone molecules in a protic solvent such as water…

Q: 13. The alkyl radical formed when a hydrogen atom is being removed from the second carbon of a…

A: 13. Option C is correct.

Q: Which alkene is the most stable A D

A:

Q: The reaction scheme below shows the reactions of alkene B. Reaction II Reaction I Reaction III C + D…

A:

Q: 8

A:

Q: What alkylborane is formed from hydroboration of each alkene? CH3 c=CH2 b. CH2 a. C. CH3

A: The first step in hydroboration reaction is the addition of H and BH2 to the π bond of the alkene…

Q: What alkene can be used to prepare each alkyl halide or dihalide as the exclusive or major product…

A: Alkene reacts with chlorine to give dichloroalkanes. Thus, cyclohexane reacts with chlorine to give…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: The reaction is carried by Sandmeyer's reaction  Diazotisation of aniline followed by cuprous…

Q: Which alkene reacts faster with HBr? Explain your choice.

A: Conjugation occurs when the p-orbital of two or more than two atoms undergo overlapping. This makes…

Q: a.) Classify the following carbocations (1º, 2º, or 3º). b.) Encircle the carbocation/s that can…

A:

Q: Draw the products of each combustion reaction.

A: The alkanes (hydrocarbons) generally react with oxygen and yields carbon dioxide (CO2), as well as…

Q: ose the best starting alkyne for the reaction in the im

A: Various organic compounds are converted to other organic compounds with the help of some reagents.

Q: III II Which alkene is least stable?

A: Stability of alkene increases with the increasing number of substitutents. So, greater the number…

Q: Consider the conversion of alkyl halide A to ether B. Question: Classify the conversion of A to B as…

A: A reaction in which one group or atom is replaced by other atom or group is known as substitution…

Q: a terminal alkene that

A:

Q: КОН CH3(CH2)16C ОН

A: The given compound is an acid. It will react with KOH to given potassium salt of acid and H2O.

Q: What alkene can be used to prepare attached alkyl halide or dihalide as the exclusive or major…

A: When a protic acid (HX) is added to an asymmetric alkene, the acidic hydrogen attaches itself to the…

Q: H;C-CH- -CH2- -CH2 CH3 CH3 Common Name 5. What resources could potentially be used to stabilize a…

A: Common name :- Propyl isobutyrate

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A:

Q: Draw and name alkynes and theirderivatives.

A: Interpretation: The names of alkynes and their derivatives are to be drawn.

Q: H;C „CH3 ? CH3 starting material final product

A:

Q: Chemistry Question

A: The answer to the following question is- The reactions are addition reaction in which hydron atom…

Q: Convert alkene A into alkyne B by a stepwise method.

A: Given:

Q: What is the general format of a reagent for the reaction of an alkene or alkyne to count as…

A:

Q: Draw the two addition products formed when the alkene shown below reacts with HCI and circle the one…

A: The given reaction is the addition of HCl to the alkene. According to Markovnikov’s rule, the…

Q: IV II ||

A:

Q: The most stable carbocation a

A: A carbocation is a planar molecule in which a carbon atom has a positive charge and three bonds.

Q: Explain the characteristics of electrophilic addition of HX to alkenes ?

A: GIVEN: The determine the characteristics of electrophilic addition of HX to alkenes Explanation:…

Q: 4. Show how to make each compound from an alkene (pay attention to regiochemistry) LOH OH

A: We have to draw the structures of the starting alkenes. And also we have to give the reagents.

Q: Draw the products of each combustion reaction.

A: In the presence of excess oxygen, propane burns to form water and carbon dioxide. Write the…

Q: What alkene is the major product formed from attached alkyl halide in an E1reaction?

A: Elimination reaction (1) : Elimination reaction or E1 reaction a unimolecular elimination reaction…

Q: Match each item to a choice: H3C CH3 H3C CH2 H2C: CH3 Choices: : diyne : conjugated diene : trans…

A: Diyne means any compounds having two acetylene group. Conjugated diene means any two double bonds…

Q: Alkenes are inherently reactive because...? A) The electrons in n bonds are not as stable as in o…

A:

Q: Which alkene reacts faster with HBr? Explain your choice.

A: Hydrogen bromide reacts with an alkene to form alkyl bromide. The reaction completes in two steps…

Q: It is sometimes necessary to isomerize a cis alkene to a trans alkene in asynthesis, a process that…

A: A cis alkene can be converted to trans alkene by the following steps: 1) Cis -2-butene is treated…

Q: Consider the energy diagram shown below when answer questions A- В C D FG E Progress of Reaction (a)…

A: The given energy diagram is shown below :

Q: 8. Choose the most stable alkene from each group: a. b.

A: Note: According to our guidelines we are supposed to answer only first question

Q: 3. Indicate the reagents needed to produce the given alkene as the major product. Br

A: Yes, we ca use  E2 stereochemistry This is because E2 elimination. And E2 elimination are…

Q: When doing a dehydration, the product will have the __ (more/less) substituted alkene.

A: Alkene - Alkenes are hydrocarbons having atleast one carbon-carbon double bond.  Dehydration…

Q: Axial alcohols are oxidized faster than equatorial alcohols by PCC and other Cr6+ oxidants. Which OH…

A: Three-dimensional structure of the molecules show how the possible arrangements actually are: a) The…

Q: Explain Stability of Alkenes ?

A: A type of hydrocarbon that has carbon-carbon double bond in them is alkene. The general formula of…

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.