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Many planets in our solar system contain organic chemicals including methane
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Chemistry: Structure and Properties
- The study of carbon-containing compounds and their properties is called organic chemistry. Besides carbon atoms, organic compounds also can contain hydrogen, oxygen, and nitrogen atoms (as well as other types of atoms). A common trait of simple organic compounds is to have Lewis structures where all atoms have a formal charge of zero. Consider the following incomplete Lewis structure for an organic compound called histidine (an amino acid), which is one of the building blocks of proteins found in our bodies: Draw a complete Lewis structure for histidine in which all atoms have a formal charge of zero.arrow_forwardWrite all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure as benzene. In all structures, keep the CCl bond as a single bond. Which resonance structures are the most important?arrow_forwardThe equation for the combustion of gaseous methanol is 2 CH3OH(g) + 3 O2(g) 2 CO2(g) + 4 H2O(g) (a) Using the bond dissociation enthalpies in Table 8.8, estimate the enthalpy change for this reaction. What is the enthalpy of combustion of one mole of gaseous methanol? (b) Compare your answer in part (a) with the value of tHcalculated using enthalpies of formation data.arrow_forward
- In which of the following molecules does the sulfur have an expanded octet? For those that do, write the Lewis structure. (a) SO2 (b) SF4 (c) SO2Cl2 (d) SF6arrow_forwardBond Enthalpy When atoms of the hypothetical element X are placed together, they rapidly undergo reaction to form the X2 molecule: X(g)+X(g)X2(g) a Would you predict that this reaction is exothermic or endothermic? Explain. b Is the bond enthalpy of X2 a positive or a negative quantity? Why? c Suppose H for the reaction is 500 kJ/mol. Estimate the bond enthalpy of the X2 molecule. d Another hypothetical molecular compound, Y2(g), has a bond enthalpy of 750 kJ/mol, and the molecular compound XY(g) has a bond enthalpy of 1500 kJ/mol. Using bond enthalpy information, calculate H for the following reaction. X2(g)+Y2(g)2XY(g) e Given the following information, as well as the information previously presented, predict whether or not the hypothetical ionic compound AX is likely to form. In this compound, A forms the A+ cation, and X forms the X anion. Be sure to justify your answer. Reaction: A(g)+12X2(g)AX(s)The first ionization energy of A(g) is 400 kJ/mol. The electron affinity of X(g) is 525 kJ/mol. The lattice energy of AX(s) is 100 kJ/mol. f If you predicted that no ionic compound would form from the reaction in Part e, what minimum amount of AX(s) lattice energy might lead to compound formation?arrow_forwardConsider the pyrosulfate ion, S2O72-. It has no sulfur–sulfur nor oxygen–oxygen bonds. (a) Write a Lewis structure for the pyrosulfate ion using only single bonds. (b) What is the formal charge on the sulfur atoms for the Lewis structure you drew in part (a)? (c) Write another Lewis structure using six bonds and two O—S bonds. (d) What is the formal charge on each atom for the structure you drew in part (c)?arrow_forward
- NASA’s Cassini-Huygens mission detected a large cloud of toxic hydrogen cyanide (HCN) on Titan, one of Saturn’s moons. Titan also contains ethane (H3CCH3), acetylene (HCCH), and ammonia (NH3). What are the Lewis structures of these molecules?arrow_forwardSulfuric acid is the industrial chemical produced in greatest quantity worldwide. About 90 billion pounds are produced each year in the United States alone. Write the Lewis structure for sulfuric acid, H2SO4, which has twooxygen atoms and two OH groups bonded to the sulfur.arrow_forward3. Carbon atoms will bond with each other to form a chain, often with the peripheral atoms being hydrogen. These compounds, hydrocarbons, are organic compounds composed only of carbon and hydrogen. However, when hydrogen atoms are substituted with other elements, such as fluorine, this changes the properties of the molecule. Methylfluoride (CH3F), a substituted hydrocarbon, is used in semiconductor processing. Figure 1 depicts an incorrect Lewis structure for CH3F. (QUestion shown in photo) Which reason best explains why this structure is incorrect? a) Hydrogen lacks an octet. b) Too few electrons are used. c) Carbon cannot exceed an octet. d) Fluorine atom has too many electrons.arrow_forward
- An organic compound that is distilled from wood has a molar mass of 32.04g/mol. It’s composition by mass is 37.5% carbon, 12.6% hydrogen, and 49.9% oxygen. Draw the Lewis structure of this compound.arrow_forwardWhat possible error(s) exist in the Lewis structure (assume we are trying to represent the best possible Lewis structure for the NO₂S ion knowing N is the central atom in this polyatomic ion)? [:ö==S: N= CO :O: The best structure would have double bond and two lone pairs on each oxygen atom and a single bond with three lone pairs on the sulfur. There are no errors. This is the best possible structure. The Lewis structure above does not minimize formal charges, thus is the not the best possible structure. The nitrogen atom has an expanded octet, and this structure is impossible. The Lewis structure contains the wrong number of electrons, thus this structure is impossible.arrow_forward(a) Describe the molecule xenon trioxide, XeO3, using four possible Lewis structures, one each with zero, one, two, or three Xe—O double bonds. (b) Do any of these resonance structures satisfy the octet rule for every atom in the molecule? (c) Do any of the four Lewis structures have multiple resonance structures? If so, how many resonance structures do you find? (d) Which of the Lewis structures in (a) yields the most favorable formal charges for the molecule?arrow_forward
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