What is the systematic name for the molecule depicted by the following bond line structure? Decide what the longest C-C chain is (parent) and then decide which substituents are there and how to number it to give the lowest locants. Make sure each substituent gets a locant. Separate letters from numbers by a dash, and numbers from each other by a comma. Do not put any spaces in your name.

What is the systematic name for the molecule depicted by the following bond line structure? Decide what the longest C-C chain is (parent) and then decide which substituents are there and how to number it to give the lowest locants. Make sure each substituent gets a locant. Separate letters from numbers by a dash, and numbers from each other by a comma. Do not put any spaces in your name.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 1E

See similar textbooks

Similar questions

Interconversion of the staggered and eclipsed conformations of alkanes requires rotation around a -C bond such as the one depicted below (see arrow). Using your knowledge of bonding, explain why these rotations do not significantly affect the energy (strength) of these bonds. You may find it helpful to describe the type of bond being rotated.
Using your model of butane (CH3CH2CH2CH3) , complete the following graph of the anglebetween the two Me groups vs. potential energy. a. Label each Newman projection of butane on the graph with the words staggered, eclipsed, gauche, and anti, as appropriate. (Note that some structures will have more than one label.) b. Draw a wedge and dash bond representation of butane in its lowest P.E. conformation.
Consider the Newman projection below. a. Draw a full Lewis structure of this molecule with R1=Me,R2=Et , and R3=iPr . b. Given the sizes of these R groups (R3R2R1) , does the Newman projection above show thelowest potential energy conformation of this bond? If not, draw a Newman projectionshowing the lowest P.E. conformation (sighting down this same bond). c. To draw a Newman projection in the lowest P.E. conformation, the following rule of thumbusually applies: Place the largest group on the front carbon anti to the largest group on theback carbon. Is your answer to the previous question consistent with this rule of thumb?
Identify circle the alkanelike portions of the following molecules: a. b. c. d.
Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
How many ifs are lost from the molecular formula of pentane if the ends are joined into a ring(changing the parent name of the molecule to cyclopentane)?
Which of the following alkenes have the Z designation? Choose all that apply.
Provide the best IUPAC name for the following molecules in the images below
Choose a likely identity for X, Y, and Z in these structures. see attached
I know the answer is correct but I can’t figure out if C is tertiary ? It can’t be secondary because it has more than two carbons connected to the +C
Please help , will provide helpful ratings for solving all 4 subparts only. Draw the skeletal structures that correspond to the following systematic (IUPAC) names.
For the following molecule, give, according to IUPAC standards, it's name. Follow the rules for commas, spaces and dashes. Be sure to indicate which center the R/S configuration applies to.