Can you please show step by step how to rank the atoms surrounding the chiral centers to determine if the configurations are R or S? For example, for NH2- The N attached to C should be 1 I believe The H attached to that C should be 4 I believe The C closer to the alkyl group should be ___________ and why that is___________. The other C should be ________ and why that is ________________.

Can you please show step by step how to rank the atoms surrounding the chiral centers to determine if the configurations are R or S? For example, for NH2- The N attached to C should be 1 I believe The H attached to that C should be 4 I believe The C closer to the alkyl group should be _____ and why that is_. The other C should be and why that is ____________.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter12: Chirality

Section: Chapter Questions

Problem 2E

See similar textbooks

Similar questions

1.Circle the organic the functional groups and name them. 2.Mark all chiral centers and determine the configuration of one of them.
Circle and name three functional groups within the molecule and place an * against any chiral carbons
Consider the molecules shown here. Assign the R/S configuration to each chiral center.
Determine the R/S configuration of each chiral center in the molecules shown below. (Do not include lone pairs as an attachment when identifying the chiral centers.)
Please also point out where the chiral centers are.
For the compounds shown, use the R/S configuration given in the compound name to finish drawing the structure by changing bonds to the the appropriate wedge‑and‑dash bonds. For each compound, change two of the in‑plane bonds to a wedge and a dashed bond. You can select the chiral bond and click on top of an in‑plane bond to quickly modify it.
Circle the chiral molecules below. Please provide an explanation for each molecule.
hey could someone help me label all of the chiral carbons as R or S? Thanks!
In the structure below, click on each of the chiral centers.
4. (a) How many chiral carbons are present in the compound below in the picture? Mark the chiral carbons with an asterisk (*). (b) How many total optical isomers are possible for the structure below in picture? 5. Identify the functional groups in the molecules shown below.
CANNOT BE HAND DRAWN! Please help correct my work Determine if your molecule contains any chiral carbons. If there are chiral carbons in your molecule, circle or highlight all of them. If your molecule does not contain any chiral carbons explain why none of the carbons are chiral.
Why are the chiral carbons (S) and (R)? Shouldn't they be both (S)?