For each of the alkyl bromides, do think it is likely to form the you substitution or elimination product? Write a sentence or two for each. Br Br -OMe or

Q: The reaction below is known as the haloform reaction. Why do only methyl ketones form a haloform?…

A: Haloform reaction: The haloform reaction is the reaction of methyl ketone with halogen (chlorine,…

Q: The electrostatic potential maps of benzene and pyridine are shown here. Is the electrostatic…

A: Electrostatic potential map tells us about the charge distribution within a molecule. By knowing…

Q: How To Assign the Prefixes E and Z to an Alkene ? discuss by steps ?

A: E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.

Q: The benzylic position has unique reactivity and resonance stability. Which structures can this…

A:

Q: Nucleophilic attack may appear to occur in two steps as shown below. The alcohol is the nucleophile…

A: The carbon atom double bonded to oxygen atom and single bonded to two alkyl groups is called…

Q: Show all the steps necessay,in order to make each of the followring compoundS, Starting with benzene…

A: Preparation of 2,4-Dibromobenzoic acid from benzene can be done as follows:

Q: Which one should be considered the major kinetic product of the following reaction?

A: Alkadienes electrophilic addition reactions 1. 1,2-addition : At lower temperature conditions…

Q: Please write the missing reagent(s) over the arrow after analyzing the functional group(s) in…

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Q: This is a hydrogenation and carbene addition problem. How do I draw the structure of the major…

A: Interpretation: We have to write the product for the following reaction.

Q: The replacement of bromide ion to the iodide ion as a leaving group in the substitution reaction…

A: In the given problem, the nucleophile attacking is OH- and the leaving groups are Br and I. Since,…

Q: My question is still the same, What is the major substitution product of the reaction, and what is…

A: The replacement of any atom or group of atom by a nucleophile is termed as nucleophilic substitution…

Q: Why substitution and/or elimination of the phenolic hydroxyl group does not occur?

A: Phenol is an aromatic compound with the hydroxyl group on benzene. Phenol is the derivative of…

Q: Draw the mechanism for the conversion of propanedial (see Problem 7.43) in its keto form to its enol…

A: The given compound is propanedial, and it is in keto form as shown below:

Q: Increasing alkyl substitution stabilizes an alkene by an electrondonatinginductive effect. Explain ?

A: Alkene are hydrocarbon having carbon - carbon double bond . Increasing alkyl substituents ,…

Q: Please solve for the following Stretter Reaction showing the steps and the final product.

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Q: Is the following true or false? When you consider the normal polarity of a carbonyl molecule it…

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Q: Please explain the reaction mechanism above to show how product is formed. The product is the borate…

A: Polymerization is a process in which the monomer units are combined together to furnish a…

Q: Draw the structure of the alkene that will give the alcohol in Figure 10 as the main product.

A: It is an example of electrophilic addition reaction

Q: Refer to the HBr- ---

A: ->Because free radical initiator or peroxide not present .Hence, there occur Markovnikov's…

Q: The electrostatic potential maps of benzene and pyrrole are shown here. Is the electrostatic…

A: The red color in the electrostatic potential map represents the high electron density or an…

Q: What is the curved arrow notation for the formation of the following alkene?

A:

Q: List reasons why substitution is difficult on accomplish on the benzene ring?

A: in substitution reaction,  either nucleophile or electrophile can attack at substrate and substitute…

Q: ) Complete the following Oxymercuration-demercuration reaction. (Pay attention to the…

A: In oxymercuration and demercuration (OMDM) an alkene is treated with Hg(OAc)2 and the product is…

Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the missing…

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

Q: What would be the steps needed to transform the first molecule into the second molecule?

A: On bromination in the presence of light, methylcyclopentane is converted to…

Q: This following reaction is considered:

A: Given : reaction

Q: Which of the following is a proper and reasonable resonance hybrid structure of benzaldehyde that…

A: When a molecule (or) ion can not be represented by single lewis dot structure and more than one…

Q: NH2 Br 1

A: In the given chemical reaction the amino group attached with the benzene ring is replaced by the…

Q: For the boxes on top of the arrow, fill in the reagent(s) and solvent(s). -SiMe3 BY

A:

Q: A. intermediate. alkyl halide is most likely to the

A:

Q: Give a clear handwritten answer of this reaction Draw the condensed of line angle structure formula…

A: Saytzeff's Rule: H+ will be eliminated from that ẞ-carbon from where the most substituted alkene is…

Q: Show the complete reaction mechanism that would make N-butylhexanamide from butane.

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Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.

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Q: The first alkene which requires the position of the double bond to be indicated is?

A: Alkene contains a carbon-carbon double bond and for this minimum two carbon atoms are required.

Q: 1) Which one more reactive to word nucleophilic substitution P- nitro toluene or O- ethyl toluene ?…

A: P-nitro toulene will be more reactive towards nucleophilic substitution than O-ethyl toulene because…

Q: Both questions help please 1) ‘When a hydrogen halide adds to an asymmetrical alkene, the addition…

A: IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds

Q: Decreasing order of electrophilic substitution reaction for the given compounds is

A: To find: The decreasing order of electrophilic substitution reaction for the given compounds

Q: QUESTION 10 Use Hammond's postulate to determine which alkene in each pair would be expected to form…

A: The carbonation which is more stable will form faster to give the product .

Q: he electrophilic addition reaction shown below involves a carbocation rearrangement. (First Image)…

A: The given carbocation in the mechanism step is tertiary, so, no more rearrangement can be possible.…

Q: Complete this concept map to summarize all epoxide reactions: CH3 CH₂ НО. Weak Nuc, H₂O+ CH3 H3C 1.…

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Q: Draw the structure of the alkene that will give the aldehyde in Figure 8 as the only organic product…

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Q: This question refers to the following reaction:          i) Determine whether the main reaction to…

A: Substitution or elimination depends on nucleophile if which OH- is from H2O then there will be…

Q: Predict the product or starting material of the following alkene addition reactions. Remember,…

A: According to Markovnikov's rule, during the addition of hydrogen halide to unsymmetrical alkene, the…

Q: Using the principles described in this course, explain (using sentences and drawings) why…

A: The more stable the carbocation ,the lower the activation energy for reaching that inter mediate…

Q: H-CI

A: Protonation of alkene give more stable carbocation. Addition of chloride ion to carbocation gives…

Q: Complete the reaction that is shown in the picture below.

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Q: ? CH, Hint Remember that overalkylation is a problem when it comes to Friedel-Crafts

A: Friedel-Crafts alkylation is the process of replacement of an aromatic proton by an alkyl group and…

Q: Please help. What other combination of ylide and aldehyde or ketone will give methylenecyclohexane…

A:

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.