Draw the two possible products formed when this diene reacts with HBr. Do not include any byproducts formed.

Q: Predict the starting alkyl bromide that would produce the product shown in the SN1 reaction. Assume…

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Q: You can identify relative strengths of acidity of molecules using key factors such as those in the…

A: This question is based on acidic strength of carboxylic acid.

Q: siven the reaction below. Which of the pairs represents and acid and it conjugate base? HSO4¯ +…

A: In the Brønsted-Lowry definition of acids and bases, a conjugate acid-base pair consists of two…

Q: A ¹H NMR spectrum is shown for a molecule with the molecular formula of C4H8O. Draw the structure…

A: NMR stands for Nuclear Magnetic Resonance, which is a technique used in chemistry and physics to…

Q: Draw the major product formed when 13- pentadiene reacts with this acid. Do not include any…

A: An addition reaction is a chemical reaction in which two or more reactants combine to form a single,…

Q: Draw the two possible products of this reaction. Ignore inorganic byproducts.

A: The hydrogen atom present on the carbon atom adjacent to the carbonyl carbon is acidic in nature.…

Q: Identify which of the following compounds CANNOT be classified as a Bronsted-Lowry base: H3C Na IV…

A: Bronsted–Lowry base is a proton acceptor. Bronsted-Lowry Acid is a proton donor.

Q: Draw the skeletal (line-bond) structure of CH3CH2CHCH(OH). Include all lone pairs and charges as…

A: The skeletal structure represents the series of atoms that bonded together to form the essential…

Q: Draw the major product of the aldol condensation reaction between two of these aldehydes with the…

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Q: In the circled atom in this structure. CH3 A) four sigma bonds B) three sigma bonds, one pi bond and…

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Q: 6. Which of the following diagrams illustrate(s) an improper way of spotting a TLC plate? Tell what…

A: In order to spot in TLC properly several rules should be followed.  1. The spots should be above the…

Q: Draw the major product of the aldol addition reaction between two of these ketones with the…

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Q: Draw the tautomer of this aldehyde. Include all lone pairs. Ignore inorganic byproducts. H3O+…

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Q: Draw the missing organic products in the following multistep synthesis. Ignore any inorganic…

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Q: This dienol readily reacts under acidic condiuchs. Draw the product of this reaction. Include all…

A: Alcohol  becomes dehydrated when it combines with protic acid to lose water molecules while being…

Q: Cyclohexa-2,4-dien-1-one will quickly undergo an acid-base reaction. Draw the initial aromatic…

A: This reaction is proceed by forming a enolate ion which is further resonance stabilized and then…

Q: Starting from the wedge-and-dash structure below, rotate the back carbon to provide the Newman…

A: The Newman projection represents the dihedral angle and the different conformations of the molecule.…

Q: Two fractionating columns are each 40 cm in length. Column A has 20 cm. By marking in the space…

A: Given, Length of fractionating column , L = 40 cm HETP of column A =  2cm HETP of column B = 20 cm

Q: Use your understanding of the key factors that influence acidity to choose the most acidic proton on…

A: Given that, a structure of a molecule is We have to determine the most acidic proton on the given…

Q: c) The combination of formic acid and methyl amine r combined with phenylacetone, a schedule…

A: Step by step mechanism.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. I + I 1 H3O+

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Q: Describe three ways in which colorless compounds can be located on a TLC plate.

A: Thin layer chromatography (TLC) : TLC plate is made of sheet of aluminium foil, glass on which a…

Q: Draw the major product of the aldol condensation reaction between two of these aldehydes with the…

A: Aldol condensation: Two carbonyl compounds joined together by the formation of a carbon-carbon bond…

Q: Draw the major product of the aldol condensatio reaction between two of these aldehydes with th…

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Q: Cycloheptatriene (shown below) is non-aromatic because it A) does not have 4n+ 2 pi electrons. B) is…

A: For compound to be aromatic it must be Cylic Planer Fully conjugate  Contains (4n+2) pi electrons.…

Q: Br CH3OH heat

A: For the given E1-elimination reaction, rearrangement of the carbocation will occur and the major…

Q: The image below shows a portion of a 'H NMR spectrum (ppm). Choose the partial structure that best…

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Q: Draw the triol needed to produce the carbonyl product under the conditions shown.

A: Na2Cr2O7/H2O, CH3COOH can only oxidize primary and secondary alchohol. primary alchohol to…

Q: Draw the enolate anion and the ester that would be needed to make this product through a Claisen…

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Q: 1: The following TLC plate was prepared with the stationary phase as silica gel (polar, SiO₂) and…

A: In thin-layer chromatography, the retention factor (Rf) is used to compare and help identify…

Q: Do the "-ed Suffix" Activity Underline the baseword and circle the suffix in each word below. Read…

A: Please find the below answer of this question.

Q: Draw the major 1,2- and 1,4-addition products ormed when this diene reacts with HBr. Do not include…

A: Given : structure of reactant.  Tip : stability of carbonation.             3° > 2° > 1°

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: The base(NaOH) can also acts as a nucleophile to attack the carbonyl carbon of the ester. First OH-…

Q: Draw the major product of the aldol addition reaction between two of these ketones with the…

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Q: Draw two major products of this reaction. Use wedge and dash bonds to indicate stereochemistry where…

A: Given reaction is hydrolysis of alkene. Alkene on hydrolysis gives alcohol as major product.  This…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: We have been given reactants and products.We have been asked to draw curved electron pushing arrows…

Q: 8. For each molecule below determine the number of peaks you would observe in the 'HNMR 13CNMR,…

A: Chemically equivalent protons or carbon show only one peak  Chemically non equivalent protons or…

Q: What difficulty may result if a. chromatographic column is not placed in a vertical position? b. the…

A: Column chromatography.

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.