The structure of the sex attractant of the common housefly, cis-9-tricosene is to be drawn. Given tricosane is the straight chain alkane with molecular formula C 23 H 48 . Concept introduction: The number of the carbon at which the double bond starts is given before the name of the parent. The isomer in which the substituents are present on the same side of the double bond is called the cis isomer. To draw: The structure of the sex attractant of the common housefly, cis-9-tricosene. Given tricosane is the straight chain alkane with molecular formula C 23 H 48.

Question

3. Assign absolute configuration (Rors) to each chirality center. a. H Nitz C. он b. 0 H-C. C H 7 C. ་-4 917-417 refs H 1つ ८ ડુ d. Но f. -2- 01 Ho -OH 2HN

Answer 1

Question

Chapter 7.4, Problem 8P

Interpretation Introduction

Interpretation:

The structure of the sex attractant of the common housefly, cis-9-tricosene is to be drawn. Given tricosane is the straight chain alkane with molecular formula C₂₃H₄₈.

Concept introduction:

The number of the carbon at which the double bond starts is given before the name of the parent. The isomer in which the substituents are present on the same side of the double bond is called the cis isomer.

To draw:

The structure of the sex attractant of the common housefly, cis-9-tricosene. Given tricosane is the straight chain alkane with molecular formula C₂₃H_48.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

3. Assign absolute configuration (Rors) to each chirality center. a. H Nitz C. он b. 0 H-C. C H 7 C. ་-4 917-417 refs H 1つ ८ ડુ d. Но f. -2- 01 Ho -OH 2HN

How many signals do you expect in the H NMR spectrum for this molecule? Br Br Write the answer below. Also, in each of the drawing areas below is a copy of the molecule, with Hs shown. In each copy, one of the H atoms is colored red. Highlight in red all other H atoms that would contribute to the same signal as the H already highlighted red. Note for advanced students: In this question, any multiplet is counted as one signal. Number of signals in the 'H NMR spectrum. For the molecule in the top drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in top molecule For the molecule in the bottom drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in bottom molecule

In the drawing area below, draw the major products of this organic reaction: 1. NaOH ? 2. CH3Br If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. No reaction. Click and drag to start drawing a structure. ☐ : A ค