1. Complete the following reactions, with the major organic product. a. CH3-CH=CH2 + Br2, b. + Br2

Q: Can you explain part d please? why do we put ethyl in the beginning?  Also in my answer key for…

A: According to IUPAC nomenclature is an organic compound is named by identifying molecule's longest…

Q: Show the organic product formed when 4-methylpentanal is heated with sodium methoxide in methanol as…

A: We will find out the reaction product

Q: to carry out the following conversion. Then, perform an additional reaction, continuing onto the…

A: A less substituted alcohol can be made from an alkene by doing the Hydroboration-oxidation reaction.…

Q: Considering these four types of alkyl halides, primary, secondary, tertiary, and methyl, which kind…

A: We know that SN2 reaction : the SN2 reaction proceed in one step and it is second order reaction it…

Q: give the major products of each reaction

A: We have given three organic reactions.  Major product : the major product of reaction is the product…

Q: two examples each of Unsymmetrical alkenes and reagents

A: Alkenes having different groups attached to either end of the carbon - carbon double bond are called…

Q: The least Stable carbocation is

A: Given that : We have to identify the least stable carbocation out of the following :

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism.

A:

Q: Need help with this SN2 esterification reaction mechanism with pushing arrows. Please help.

A:

Q: In the lab, a student desires to obtain compound A but instead always getting compound B as the…

A: It is an electrophilic aromatic substitution reaction.

Q: Supply synthetic routes to the following molecules using the indicated starting materials

A: The synthetic route for preparation of 2-hexanol is as follows,

Q: Finish the synthesis by listing out the reagents/solvents used and draw intermediate structures.…

A: Here we have to synthesize 4-ethylcyclohexan-1-one from the given starting material by multistep…

Q: Terminal alkynes when reacting with a base such as sodamide (NaNH2), what do they become? This what…

A: Terminal alkyne contains an acidic hydrogen atom. This hydrogen atom is removed as a proton to form…

Q: NO2 CI

A:

Q: During benzoic acid synthesis, the Girgnard reagent is formed when this atom ______ inserts itself…

A: In the synthesis of benzoic acid using Grignard reagent, the reactant used is CO2.

Q: Give two (2) examples of reactions for each of the types of organic reactions: substitution,…

A:

Q: What type of synthesis is this an example of?  Is this showing the addition of a ketone giving a…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: In this short synthetic sequence, provide the organic structures of the missing reactant and the…

A:

Q: Give two examples each of Unsymmetrical alkenes and reagents and give two examples of reactions of…

A: Unsymmetrical Alkene Unsymmetrical alkene is those alkenes in which double-bonded carbon atoms have…

Q: what one compound would I use as a starting point for the attached reaction?

A:

Q: NaNH2 CH;-I H20 CH3-CECH A в Hg2“, H*

A:

Q: raw the major product of the SN2 reaction below ar roduct formation. Remember to consider product st…

A: For the E2 elimination, leaving group and H on beta carbon should be anti-periplanar.

Q: Are terminal alkynes considered weak or strong acids? Explain why.

A: Welcome to bartleby !  Introduction :  We have to tell terminal alkynes are weak or strong acids .

Q: Choose the reagent(s) that would be most likely to complete this reaction. Br

A:

Q: Using the Strecker Reaction, please show the steps and the final product of the following reaction:

A: Strecker synthesis is preparation of alpha- aminonitriles which are intermediate for the synthesis…

Q: Draw the most stable carbocation that can be formed by the compound in Figure 5.

A: A carbocation is for when a carbon atom acquires a positive charge, The shape of a carbocation is…

Q: Add curved arrows to the structures shown below in order to complete the mechanism. OCH3 OCH3 НА OH…

A:

Q: Please design syntheses that convert the starting materials on the left to the products on the…

A: Following is the synthesis of the given product from the starting material.

Q: CI BAC

A: This reaction results in the formation of amide.

Q: 1. Which alkene is the major product of this dehydration?

A:

Q: Form benzene, phtalic anhydrous, compunds with 6 carbons or less and any inorganic reagent you want…

A: In the given problem we have to synthesize a given molecule from the benzene, phthalic anhydrous,…

Q: What type of carbocation is shown? (+)

A:

Q: True or False for the product of this reaction. HOOCCH CH>COOH + Heat --> Cyclic dicarboxylic acid

A: The reaction taking place will be as shown below.

Q: Hi please show your working out and make comments about what you are doing and why. This question…

A: Intermolecular forces refer to the type of interactions which are present in between atoms or…

Q: Show the Complete halogenation of CH4 using excess Cl2 ?

A: Halogenation is a chemical reaction involving the addition of one or more halogens to a compound or…

Q: Draw and name the organic product of the given reaction. Select Draw Rings More Erase H, SO, + ΗΝO +…

A: Benzene generally under go electrophilic substitution reactions.  Some important electrophilic…

Q: 2. Draw the major product of this SN1 reaction. Ignore any inorganic byproducts. он HBr

A:

Q: [References Draw the major organic product of the following reaction. Li Cul Br pentane A? B? • In…

A: Ans

Q: What methods introduce the functional groups in the product ?

A: Functional groups are the atoms or cluster of atoms that determine the physical and chemical…

Q: octane from 1-butene

A: The structure of 1-butene is shown below. The structure of octane is shown below.

Q: CH3-C=CH А B Hg2*, H*

A: Terminal alkynes on reaction with sodium amide(NaNH2) produces corresponding acetylide which attacks…

Q: Br CH;CH,OH

A: CH3CH2OH is neutral base and compound is 3 degree halide compound. So the reaction occurs via E1…

Q: Choose the reagent(s) that would be most likely to complete this reaction.

A: Given: reaction of formation of 2-pentanol from pentene. To find: suitable reagent for this…

Q: raw the major organic product of the SN1 reaction:

A: Carbocation can be defined as the molecule in which a carbon atom carries positive charge.

Q: Based on the hydrogenation and the bromination reaction information, how many different alkene…

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

Q: Choose one example from the set of synthesis reactions in Model 1

A: In model-1 there is a different types of chemical reactions are given 1. Combination reactions ( set…

Q: Please propose a synthesis of the target molecule using as many steps or reagents and answer these…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: What type of carbocation is shown?

A: As we can clearly see that the positive charge (cation) containing carbon is attached to two carbon…

Q: How Electron-withdrawing groups destabilize the carbocation ?

A: The electron withdrawing groups (must contain an electronegative atom) are those which has tendency…

Q: но, b) H

A:

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.