18. Carbon dioxide is non-polar, despite the fact that oxygen is much more electronegative than carbon. Briefly explain why, using relevant diagrams as appropriate to illustrate your answer.
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- pls help ASAP! “which term best describes the relationship between the following two molecules?”Select all of the following that have permanent dipole moments (i.e., they are polar). -BCl3 -PCl3 -CH3OCH3 (an ether) -C3H8Polarity (a 3-d representation with bond and molecular dipoles annotated) of ClO4- , PF3, H2O, PF5 , SF4
- draw diagram that best describes the orbitals involving non-hydrogen bonds in C H3 O H?Statement 1: The boiling point of compound2 is lower because of the number of bondingregions present Statement 2: Moreover the increased no. of sigmabonds result to more difficult distortion resulting to a stronger attractive force within the atoms prensent Which is true? Statement 1, 2, both, or noneConsider the following orbital representation of HCCH (ethyne). a. Answer the same three questions (a-c) from the previous exercise. b. Label each CH bond in the drawing above. c. What is the total number of a bonds found in ethyne?…. bonds? d. How many p orbitals are there on a single carbon of ethyne? e. How many hybrid orbitals are there on a single carbon of ethyne?
- Using your model of butane (CH3CH2CH2CH3) , complete the following graph of the anglebetween the two Me groups vs. potential energy. a. Label each Newman projection of butane on the graph with the words staggered, eclipsed, gauche, and anti, as appropriate. (Note that some structures will have more than one label.) b. Draw a wedge and dash bond representation of butane in its lowest P.E. conformation.Consider the incomplete orbital representation of O2 , below right. a. Identify which lobes are hybrid orbitals (identify the type) and which lobes arep orbitals. b. Use dotted lines to show any bonds. c. Use up or down arrows to show electron occupation of each hybrid orbital or bond.Organic chemistry is a bit like cooking. Later in this course we will study “recipes” for preparingnew molecules. A common instruction in such recipes is “add a strong acid” or “add a strongbase” (rarely are they added at the same time since a violent reaction ensues). You will see theseterms frequently from now on, and are expected to be able to recognize them or draw theirstructures from memory. Memorize them before next class.
- Propanal (bp 48°C) and propanol (bp 97°C), both found on Table 4.2, have very similar surfaceareas and dipole moments. Construct an explanation for the large difference in boiling pointsbetween the two.I NEED ANSWER FOR NUMBER 3. Find the following in each compound :A. Draw the overlapping of orbitalsB. Identify the hybrid orbitalC. Identify the molecular orbital__ Al(OH)3 + ___ HBr ------> ___ AlBr3 + ___ H2O Can yo balence this for me