Chapter 4: 4-21 (page 90)
Look at the following structure of the female hormone estrone, and tell whether each of the two indicated ring-fusions is cis or trans.

Short Answer
Both structures have trans-ring fusions.
/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none}
Learning Materials
Features
Discover
Chapter 4: 4-21 (page 90)
Look at the following structure of the female hormone estrone, and tell whether each of the two indicated ring-fusions is cis or trans.

Both structures have trans-ring fusions.
All the tools & learning materials you need for study success - in one app.
Get started for free
Which is more stable, a 1, 4-trans disubstituted cyclohexane or its cis isomer?
Give IUPAC names for the following cycloalkanes

Draw the more stable chair conformation of the following molecules, and estimate the amount of strain in each: cis-1-Bromo-4-ethylecyclohexane.
Name the following substances, including the cis- or trans- prefix (redbrown= Br):

Hydrocortisone, a naturally occurring hormone produced in the adrenal glands, is often used to treat inflammation, severe allergies, and numerous other conditions. Is the indicated group axial or equatorial?

What do you think about this solution?
We value your feedback to improve our textbook solutions.