Specific rotation of glucose molecule (anomers)

Q1. α-D-Galactopyranose has [α]D = +150.7o, and β-D-galactopyranose has [α]D = +52.8o. When either of them is dissolved in water and allowed to reach equilibrium, the specific rotation of the solution will be +80.2o. What are the percentages of each anomer at equilibrium? I really have no ideal how ...continues

Reaction mechanism (epoxide + alcohol)

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Multistep synthesis

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Reaction mechanism (carboxylic acid + alkyl anion)

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Reaction using NaBH4

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Organic Chemistry - Molecules

Organic Chemistry - Molecules. Please see the attached file for full problem description.

synthesis

synthesize the following product using: any organic compound with 3 or less carbons, N-bromosuccinimide, triphenylphosphine, m-chlorobenzoic acid or ANY inorganic reagent.

Chemistry/Organic

Draw the structure of the major organic product for each of the reactions shown below. If you can show stereochemistry, where relevant will help me out. Please see the attached file for full problem description.

organic chemistry structural problem with for Methyl Ketone

In organic chemistry, there is a ketone structure that has the carbon bonded twice with the oxygen(C=O)with two components on the side, R C=O / R' the question is how or where do I atta ...continues

Stereochemistry

Draw the possible chair forms of cis and trans 1-isopropyl-3-methylcyclohexane. Are the two forms identical, enantiomeric, or diastereomeric? In each case, indicate which chair term will be more stable and explain why. Is either of these molecules chiral?