2.Now write the condensed formulas for the following bond-line structures.laонНHO.

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Answered: 2. Now write the condensed formulas for…

Chemistry: Matter and Change

1st Edition

ISBN:9780078746376

Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom

Publisher:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom

Chapter8: Covalent Bonding

Section8.1: The Covalent Bond

Problem 13SSC

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1. For each of the following compounds and ions, draw the complete Lewis structure. All formal charges should be on the atoms that possess that formal charge. CH4 H3CBr CH3CH₂OH H₂S H₂SO4 (sulfuric acid) H³0+ CH3* 2. Convert the following condensed formulas into bond-line structures, making sure to draw in zig-zag formation. CH3CH₂CH₂CH₂CH₂CH₂CH₂CH3 FCH₂CH₂I H₂C=CHCH₂OH (CH3)2CHCOOH
Now write the condensed formulas for the following bond-line structures.
Draw the bond-line formula for each of the following condensed structural formulas.These may go beyond the simple explanations above but you can imply the connectivity based on the atoms’ desired valence. a)(CH3)3CCH2CH3 b)(CH3)2CHOH c)(CH3)2CHOH
Part G. Molecules with Oxygen and Nitrogen. Organic molecules often contain the elements oxygen and nitrogen. Construct a model with the molecular formula C5H12O where the oxygen is bonded to one hydrogen. When a hydrogen is bonded to an oxygen or nitrogen, you need to draw that bond in a bond-line structure. Draw the bond-line structure of this model. What is the molecular geometry of oxygen in your structure? Draw three more constitutional isomers with the molecular formula C5H12O where the oxygen is bonded to one hydrogen. Structure Structure Structure Draw three more constitutional isomers with the molecular formula C5H12O where the oxygen is bonded to two carbon atoms. Structure Structure Structure
10. Name the following structure. 11. Of these two resonance structures, the greater contribution to the resonance hybrid is from the second one. Based on what you know about charge stability, does this make sense? How can you explain this observation, with everything you know about resonance forms?
I have given you a condensed structure. You need to convert it to an accurate bond-line structure. CH3 CH3-CH-CH2-CH-CH₂-C-H 12-CH-CH2₂-C-1 CI Draw (as bond-line structures) isomers of this compound where you only move the chlorine atom. Draw four isomers of the original compound that would have a five carbon chain as the longest chain. [Note: there would be many isomers that will satisfy this. Find any four.] Using the original molecule (and looking at the carbon next to the aldehyde carbonyl) what would be the charge on that carbon if I removed an H atom and left behind the pair of electrons? Circle the best answer Positive Negative Neutral In the space below, draw that structure (from the sentence above) as a bond-line structure. Then, draw a resonance structure for this ion and be sure to add curved arrows to show the movement of electrons.
Unshared, or lone, electron pairs play an important role in determining the chermical and physical properties of organic compounds. Thus, it is important to know which atoms carry unshared pairs. Use the structural formulas below to determine the number of unshared pairs at each designated atom. Be sure your answers are consistent with the formal charges on the formulas. The number of unshared pairs at atom a is The number of unshared pairs at atom b is HyC CH The number of unshared pairs at atom e is The number of unshared pairs at atom a is The number of unshared pairs at atom b is HC CH The number of unshared pairs at atom e is
Line-bond structures appear to imply that there are two different isomers of 1,2-dibromobenzene, one with the bromine-bearing carbon atoms joined by a double bond and one with the bromine-bearing carbons joined by a single bond. In fact, though, there is only one 1,2-dibromobenzene. Explain. H H. C. Br H. .C. Br || || .C and 1,2-Dibromobenzene Br Br
1. What is resonance contributor in which one or more atoms bears a formal change and the most stable resonance form? 2.what is the process of distributing electron pairs in a molecule? 3. Are organic molecules which are less sterically hindered more attractive than those which are more sterically hindered?
Fatty acids are molecules with a carboxylic acid on one end and long hydrocarbon chain on the other. The sodium salts of fatty acids (such as sodium strearate, shown below) are commonly used in soaps to trap nonpolar dirt and grease particles. Soap does not work well in "hard water, which is water with high concentration of magensium and calcium ions (often found in water obtained from wells) Explain this observation at a molecular level.
Write an equation for the reaction of CH3 SCH3 with BF3, a Lewis acid, and show by the use of curved arrows how the reaction occurs. • Show all hydrogen atoms that are not attached to a carbon atom. Apply formal charges where appropriate. Assign lone pairs and radical electrons where appropriate. • Use the "starting points" menu to revert to the original molecule(s) shown. • Draw the appropriate electron-flow arrows. • Omit+ signs between structures. ● ● CH3 | :S: | CH3 == starting points == ↑ TAYY : F کر ? ChemDoodleⓇ
What is the correct IUPAC name of the bond line structures below?

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2. Now write the condensed formulas for the following bond-line structures. la он Н HO.