option 2 is correct
Explanation: zero degree rotation of 2-bromobutane indicates the presence of racemic mixture of compounds.
If a solution of 2-bromobutane had an observed rotation of 0o, how would you label the...
Part of a stereochemistry and polarimetry lab 3. (4pts) (S)-2-bromobutane has a reported specific rotation of 23.1° and (R)-2-bromobutane has areported specific rotation of -23.1°C. A given sample had a measured specific rotation of -9.1°. a) Which isomer of 2-bromobutane is dominant? b) What is its percent enantiomeric excess (%ee)? 4. (4pts) A carbon atom is said to be stereogenic if it is bonded to four different groups. Identify the stereogenic carbons in the following compound. Circle all the stereogenic...
If pure (R)-2-bromobutane rotates light 100 degrees to the right, how much rotation would occur for a solution with 80% (R)-2-bromobutane and 20% (S)-2-bromobutane?
how would you name this compound. specifically the rotation portion(R and S) on my attempt i got mostly everything right except for the configurations. (blue ink indicates a reversal of the rotation if H isnt in the back.) s for each of the following. CHs (b) Br e following organic halide R-93) tbeane Frethy layclokyare Br Br HCKC
The observed rotation of compound Y is +4.5 when 0.1g/mL of its solution is measured in 1 dm sample tube. Calculate the specific rotation of compound Y ii Calculate the enantiomeric excess of a solution Y whose [o] is +25 i. How much of each enantiomer is present in solution Y
What observed rotation is expected when a 1.72 M solution of (R)-2-butanol is mixed with an equal volume of a 0.860 M solution of racemic 2-butanol, and the resulting solution is analyzed in a sample container that is 1 dm long? The specific rotation of (R)-2-butanol is - 13.9 degrees mL g 'dm"? Number deg
What observed rotation is expected when a 1.00 M solution of (R)-2-butanol is mixed with an equal volume of a 0.500 M solution of racemic 2-butanol, and the resulting solution is analyzed in a sample container that is 1 dm long? The specific rotation of (R)-2-butanol is –13.9 degrees mL g–1 dm–1.
What observed rotation is expected when a 1.36 M solution of (R)-2-butanol is mixed with an equal volume of a 0.680 M solution of racemic 2-butanol, and the resulting solution is analyzed in a sample container that is 1 dm long? The specific rotation of (R)-2-butanol is –13.9 degrees mL g–1 dm–1. please show all work
If you did an SN2 reaction with R-2-bromobutane what would the stereochemistry of the product be? a) R b) S c) achiral d) racemic mixture e) NA If you did an SN1 reaction with S-3-bromohexane what would the stereochemistry of the product be a) R b) S c) achiral d) racemic mixture e) NA
Please show work. I ALWAYS RATE! Thank you! What observed rotation is expected when a 1.76 M solution of (R)-2-butanol is mixed with an equal volume of a 0.880 M solution of racemic 2-butanol, and the resulting solution is analyzed in a sample container that is 1 dm long? The specific rotation of (R)-2-butanol is -13.9 degrees ml g^-1 dm^-1.
What would you have observed if you had added a concentration solution of NaCl to the CoCl2/ Co(H2O)6 equilibrium system? Explain your answer in the terms of shifts or LeChatelier's principle. A question in Chemistry Lab Book