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bryanna F.

bryanna F.

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Ronald Prasad verified

Numerade educator

Structure and Bonding Naming and drawing small alkyl substituents Add a methyl substituent at carbon #2, and an ethyl substituent at carbon #6 to this organic molecule. Be sure your answer is a condensed structure that follows all the usual rules. CH3—CH2—CH2—CH2—CH2—CH2—CH2—CH3

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David Collins verified

Numerade educator

Hydrocarbons Understanding the relative energy of rotational conformations The following diagram shows the relative energy of 1,2-dibromoethane as one end of the molecule rotates around the C1 — C2 bond: Relative Energy Relative Rotation The green eye shows how you should imagine looking down the C1 — C2 bond as you draw the Newman projection. Draw the Newman projection for a conformation of 1,2-dibromoethane that has the relative energy described by point D on the energy diagram above. If there is more than one conformation that could have energy D, you only need to draw one of them. Note: make sure to draw your Newman projection as viewed down the C1 — C2 bond (as indicated by the green eye). Select a template to begin.

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Nicole Krahulik verified

Numerade educator

Hydrocarbons Drawing Newman projections of simple organic molecules Draw a Newman projection for the conformer shown below as viewed from the right side of the molecule. The green eye shows you the direction you want to be looking at the molecule in your Newman projection. Select a template to begin.

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Nicole Krahulik verified

Numerade educator

Hydrocarbons Classifying hydrocarbons Classify each hydrocarbon in the table below. compound 1 type of hydrocarbon (check all that apply) ? alkane ? alkene ? alkyne ? normal alkane ? branched ? saturated ? unsaturated ? aromatic compound 2 type of hydrocarbon (check all that apply) ? alkane ? alkene ? alkyne ? normal alkane ? branched ? saturated ? unsaturated ? aromatic

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Nicole Krahulik verified

Numerade educator

Hydrocarbons Naming and drawing branched alkanes Write the systematic name of each organic molecule: | structure | name | | :--- | :--- | | ![](https://athena-production-image-storage.s3.amazonaws.com/2024/05/22/02/47/33/835/77833072-0000-4000-8000-000000000000/image.png) | | | ![](https://athena-production-image-storage.s3.amazonaws.com/2024/05/22/02/47/33/835/77833072-0000-4000-8000-000000000001/image.png) | | | ![](https://athena-production-image-storage.s3.amazonaws.com/2024/05/22/02/47/33/835/77833072-0000-4000-8000-000000000002/image.png) | |

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Ivan Kochetkov verified

Numerade educator

Structure and Bonding Numbering the main chain of branched alkanes For each organic compound in the table below, enter the locant of the highlighted side chain.

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Ivan Kochetkov verified

Numerade educator

Hydrocarbons Identifying primary, secondary, tertiary, and quaternary carbons Highlight in red the tertiary carbons in this molecule. Highlight the quaternary carbons in blue.

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Organic Acids and Bases Understanding the Influence of resonance on site acidity Highlight the most acidic of the H atoms shown in each molecule below. Note: if there are two or more H atoms with the same highest acidity, be sure you highlight them all. Also, don't worry about any additional H atoms that might exist but which aren't shown. You only need to find the most acidic H atoms of those that are shown.

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David Collins verified

Numerade educator

Organic Acids and Bases Drawing the mechanism of an organic acid-base reaction Complete this mechanism for an acid-base reaction by adding curved arrows.

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David Collins verified

Numerade educator

Complete this mechanism for an acid-base reaction by adding curved arrows.

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