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1. Draw Lewis Structures for the following compounds. (Be sure to minimize formal
charges and draw resonance structures where appropriate.): XeF2O, ClO4-, HNO2,
CH3CH(NH2)COOH (amino acid alanine).
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- 1. Draw Lewis structures for the following compounds. Remember to enclose ions in square brackets. On your answer sheet, state the number of valence electrons in each compound. (a) Na₂S (b) (CH3)₂S (c) KOCI List the most important (etrongnet) inMethyl isocyanate, CH3 -N= C = O, is used in the industrial synthesis of a type of pesticide and herbicide known as a carbamate. As a historical note, an industrial accident in Bhopal, India, in 1984 resulted in leakage of an unknown quantity of this chemical into the air. An estimated 200,000 people were exposed to its vapors, and over 2000 of these people died. Q.) Write a Lewis structure for methyl isocyanate and predict its bond angles. What is the hybridization of its carbonyl carbon? Of its nitrogen atom?Q7-) Fill in the blanks with the appropriate structures. OH Na,Cr,0, NH,OH.HCI H,SO, NaOAc heat
- Draw the Lewis dot structure of the conjugate base of cyclopentane by assuming all the atoms in the molecule obey the octet rule. Show all lone pairs and formal charges. Do no draw resonance structures.Draw a complete lewis structure for the CONJUGATE ACID of Nitromethane (condensed formula CH3NOOH). Draw a complete lewis structure that shows all bonds, unshared electron pairs, and minimized formal charges where appropriate.Give clear handwritten solution .....
- 16. Which of the following structures is the CORRECT resonance structure of the following. molecule: (A) (B) (C) (D) CH3- CH₂ CH3 -H CH₂CH3 CH₂CH-CH₂ CH3 CH3Q. 9a) Provide additional resonance structures for the following species. Remember to show lone pairs & formal charges where applicable + [ :N=N-F: +→ [:0-C!-O: → Q. 9b) Draw the Lewis Structure for NCCH2CO2NHCH3, determine the number of sigma bonds & the number of pi bonds present, and indicate the bond angle value around each carbon atom, each nitrogen atom, and each oxygen atom.19.) The thiocyanate ion (SCN-) has thee resonance structures. Each follows the octet rule (#1) has a sulfur to carbon single bond and a carbon to nitrogen triple bond. (#2) has a sulfur to carbon triple bond and a carbon to nitrogen single bond. (#3) has a sulfur to carbon double bond and a carbon to nitrogen double bond. Which structure is the "best" one using formal charge arguments? Group of answer choices 2 all three are equal 1 3 1 and 2 are equal
- Consider compounds A–D, which contain both a heteroatom and a double bond. (a) For which compounds are no additional Lewis structures possible? (b) When two or more Lewis structures can be drawn, draw all additional resonance structures.Doxorubicin, shown here, is an important chemotherapy drug used to treat avariety of cancers, including bladder cancer, breast cancer, and certain forms of leukemia. Doxorubicin works by binding to DNA in such a way that a portion of it penetrates the DNA double helix— a process called intercalation. During transcription— the process that forms RNA— portions of the DNA strands are temporarily separated for the base sequence to be read and then are reconnected. With bound doxorubicin, however, the double helix does not reform properly after the strands are separated, which disrupts replication— the process that forms an identical copy of DNA. Which portion of doxorubicin do you think intercalates into the DNA double helix, and why do you think it has little difficulty doing so?Based on the atom connectivity shown bellow,evaluate the four resonance structure for the thiosulfate ion S2O3 ^2-. Use curved arrows to indicate how you get from one resonance structure to another. Assign formal changes to all atoms and determine which of these resonance structure is the most stable based on a formal charge analysis Explain your answer thoroughly. Look at the picture.
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