k will readily Unexpectedly, 7-bromocyclohepta-1,3,5-triene dissolve in water. Draw the aromatic structure that forms in aqueous solution. Include all lone pairs in your structure.

Q: 5. Which of these structures can be classified as aromatic and why? III II

A: To be aromatic, an organic compound should satisfy the given below conditions. 1) Cyclic and planar…

Q: he reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. What is the structure of…

A: Given is, reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. This reaction is…

Q: Compounds X and Y both have the formula C7H₁4. Both X and Y react with one molar equivalent of…

A: The question is based on the concept of organic reactions.We need to identify X and Y.

Q: Identify the aromatic compounds. -Z: H I :Z II III and IV All of the answers are correct. I and II…

A: For a compound to be aromatic , compound should follow Huckel rule . Conditions:1) Compound should…

Q: The heats of hydrogenation of cycloheptene and 1,3,5-cycloheptatriene are 110 kJ/mol (26.3 kcal/mol)…

A: The resonance energy of 1,3,5-cycloheptatriene has to be determined and the resonance energy of…

Q: Draw a structure for each of the following compounds. You may use any acceptable style of drawing…

A: There are few things to keep in mind while drawing the structures from the name of the compound. 1.…

Q: Compound A and compound B are constitutional isomers with molecular formula C3H₂Cl. Treatment of…

A: The ratio of the product of substitution reaction to the elimination reaction depends on the…

Q: SN2 reaction is an example of a nucleophilic substitution reaction. Imagine that 1-iodobutane reacts…

A: Answer:

Q: picture of a nulene. What kind of hybridization do the two central carbon atoms have? What is the…

A: Comulene contains cumulated double bonds. When in a molecule one carbon bears two double bonds then…

Q: Explain why the bond dissociation enthalpy of a C-H bond in benzene is significantly greater than…

A:

Q: Classify each hydrocarbon in the table below.

A: Saturated hydrocarbons are those which having a single bond between two carbon atoms. Unsaturated…

Q: Question 9 antiaromatic. ASsume that each structure is as planar as possible. Assign each of the…

A: The compound is cyclic, planar, and conjugated. Total pi electrons = 8 so it follows 4n, n = 2 Thus,…

Q: 1) Draw the structures of the following compounds from the a) 5,6,7R-trimethyl-2E,5Z-nonadiene b)…

A: IUPAC nomenclature is used for the systematic naming of organic molecules.According to IUPAC…

Q: 2. A student named a compound as 3,3-dimethyl-4,4-diethylcyclohexa-1,5-diene. Even though one can…

A:

Q: Q17 Which of the following statements about aromatic compounds is not true? Aromatic rings are less…

A: A question based on reactivity of aromatic compounds. 4 statements about aromatic compounds are…

Q: Draw the structure of following compound. (2E,4E,6E)-octa-2,4,6-triene

A:

Q: Draw a structural formula for the major organic product of the following reaction: CH2Cl2, + Br2

A:

Q: Write the structure of the following compound: 2-(2-chlorophenyl)-1 -iodoethane.

A: The structure of the compound gives the arrangement of the atoms in the space. Various physical and…

Q: 6. Write the structure of the organic product in each of the following reactions. Assume only…

A:

Q: What is the IUPAC name of the following compound? CH,CH3 I

A:

Q: How many resonant structures can be written for each of the following aromatic hydrocarbons? (a)…

A: l

Q: 4-pyranone will quickly undergo an acid-base reaction. Identify the reaction conditions that will…

A: As a resonance contributor of C=OH+, protonation of the C=O oxygen on 1 results in the formation of…

Q: Based on naming branched alkyl substituents, and draw all possible alkyl groups having the formula…

A: Different organic compounds can have different molecular structures due to bonding of different…

Q: 4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will…

A: The given reaction is shown below.We have to predict the product of the given reaction.

Q: predict the organic product when 1-pentanol is heated in the presence of a strong acid, H+. Include…

A: Given: 1-pentanol is heated in the presence of a strong acid, H+.

Q: Of Hückel's original rules for aromaticity, one needed to be revised. Which one is it? The ring…

A: The important criteria for the aromaticity, such as ring must be planar, fully conjugated or pi…

Q: Compounds X and Y both have the formula C7H14- Both X and Y react with one molar equivalent of…

A: The question is based on the concept of organic reactions.We need to identify X and Y.

Q: 7. Draw curved arrows indicating the movements of electrons between the following pair of resonance…

A: Since you have posted unrelated multiple questions, hence answering only first 2 related ones.

Q: Write the structure of the following compound: 1 -Bromo-4-sec-butyl-2 -methyl-benzene.

A: Organic compounds are named according to the rules and recommendations of IUPAC. Here,we are given…

Q: Draw the structure of (Z) 2,4-dimethyl-3-octene

A: When same priority groups are on same side across the double bond, it is Z isomer.

Q: y isomers can be formed in each case? (2) Addition of HBr to 3,3-dimethyl-1-butene gives a mixture…

A: The addition of particular group without any substitution. For eg., HBr addition in a double bond.

Q: There are several aromatic compounds with the formula C3H3CI. Name those that have a trisubstituted…

A: Isomers are those which have same molecular formula but different structural formula.

Q: h of the following molecules could be considered aromatic? Assume all of the compounds are planar.…

A:

Q: Draw the structure of the organic product formed from the reaction of sodium methoxide with…

A: Nucleophilic aromatic substitution (SNAr) is a type of organic reaction in which a nucleophile (an…

Q: 2. Please draw out structure of the following compounds. 1) 2,3-Methyl-1,4-pentadiene 2)…

A:

Q: ON- HN- A C D E B

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.