Concept explainers
Interpretation:
The bond-line representation of the given molecule should be drawn in the box by considering only valence electrons.
Concept Introduction:
The distribution of electrons in atom into orbitals is said to be electronic configuration. The electronic configuration for every element present in the periodic table is unique or different.
The representation in which the bonds present between atoms are represented by lines is known as bond line representation.
Want to see the full answer?
Check out a sample textbook solutionChapter 1 Solutions
Custom eBook for Organic Chemistry
- I need help drawing the VSEPR geometry of ( CH2O), the electronic, molecular geometry, and if it’s polar. All of these get me confuse. Please helparrow_forwardFocus on the C atom on the left as the central atom. How many other atoms are directly bonded to this C atom? How many bonding domains are there on the C atom on the left? How many lone pairs of electrons are there on the C atom on the left? How many nonbonding domains are there on the C atom on the left?arrow_forwardThe resonance form that results from the curved arrows drawn in the figure isarrow_forward
- IV. Write the resonance structure that would result from moving the electrons in the way indicated by the curved arrows. Submit your answer as assignment. H2Narrow_forwardConsider this Lewis structure in the curved arrows joke. Draw the resident structure obtained by moving electrons as indicated by the curved arrows.arrow_forwardDraw the simplest set of curved arrows that shows how the structure on the left could be turned into the structure on the right. Show all lone pairs. If you need to expand part of the structure to show some lone pairs, expand it by drawing in all atoms and bond lines. CT toarrow_forward
- Give typed full explanation Look at figure 3-22 that shows the electron density that occurs abound the Si-O bond. This electron density map gives the "shape" of the O and Si atoms when they are bonded together. Think about the answer in Q9 and choose the best response below: (Select answer choice) a. This figure shows that the Si and O atoms, when they bond together, do not form spheres, which is due to the fact that the Si-O bond is strongly covalent and these shared electrons affect atomic shape. This change in shape limits the applicability of Pauling's Coordination principle since that principle is based on the geometry of perfect spheres. b. This figure shows that the Si and O atoms, when they bond together are close to perfect spheres, which is due to the fact that the Si-O bond is strongly covalent. This figure shows that Pauling's Coordination principle should apply very precisely to any substance that contains Si-O bonds c. This figure shows that the Si and O atoms, form in a…arrow_forwardIndicate if the bond is polar or nonpolar (in box). If non-polar write non-polar, If polar, show direction of dipole.arrow_forwardFollow the curved arrows and draw a Lewis structure for the resulting resonance contributor of 1,3-butadiene, adding charges and lone electron pairs to the appropriate atoms. CH2arrow_forward
- Butane is an unbranched alkane with the molecular formula C4H10C4H10. a) Draw the complete structure of butane. (Show all hydrogen atoms.) b) Draw the structure of butane in line-bond or skeleton mode. (Do not show the hydrogen atoms.)arrow_forwarda) Draw the formal charges to the molecule below. Label atleast two functional groups found in this molecule. Identify and circle the π bonds. b) Draw a curly arrow notation to show how the electrons are redistributed to show a new resonance structure in which the formal charge has moved to a different heteroatom.arrow_forwardThe curved arrow notation introduced in Section 1.6 is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions. Since each curved arrow shows the movement of two electrons, following the curved arrows illustrates what bonds are broken and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCl.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning