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A: Solution: The chemical structure of the given compound is shown below.
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Q: What is the hybridization of the central carbon atom of allene 1,2-propadiene
A: the hybridization of the central carbon atom of allene 1,2-propadiene is sp.
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A: The compound given is BBr3.
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A: sp2 hybridized carbon must be attached with a double bond.
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Q: What is the hybridization of the sigma bonding orbitals of the carbon atom?
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Q: 4. Describe the hybridization of each carbon atom in the following structure.
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Q: How many single bonds can an sp2 hybridized carbon have? O A. 4 О вз O c. 2 O D. 1
A: Since you have posted multiple questions, we are entitled to answer the first only.
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- 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.Represent the bonding in each molecule or ion by drawing the orbitals (hybridized and unhybridized) of each atom in the bond. Label the σ and π bonds and label each bond by the orbitals that it is made from. For instance, the C–H bond in CH4 would be made from the overlap of: C (sp3) – H (1 s). You may draw the hybridized sigma orbitals as sticks and the unhybridized p-orbitals as lobes for clairity and ease. a. HONO b. CH3 CCH c. C3 H4 d. C2 O4 2-VISUAL SKILLS The isomers of retinal have the same number of atoms and bonds but differ in thespatial arrangement at one carbon-carbon double bond (C“C). In each isomer, circle that C“C. Lookingat the atoms around that bond, to what atoms do the terms cis (same side) and trans (opposite side) refer?
- 3) Combine any Atomic orbitals to form Molecular orbitals assuming they fulfill the phase and energy requirement. Construct MO diagram (include AOs, MOs, pictures of each, electrons, HOMO, LUMO, B.O., and comparative energies, etc.). REMOVE an ELECTRON to form CATION Please only do part 3. The first image shows the problemIdentify the hybridization of the labeled carbons in the molecule Remdisivir. Answer all labels 1 to 10.a.Determine the number of nodes and rank them in order of increasing energy. b.Draw the p atomic orbital contributions on each carbon atom (AO mixing pattern) that would give rise to the MO. c. Based on your answer to part (c) -determine whether each MO is overall bonding, nonbonding, or antibonding. Please explain steps
- pls help ASAP! “which term best describes the relationship between the following two molecules?”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 any one of the four identical hybrid orbitals in the 109.5° set. a. What fraction of the clay in this hybrid orbital was originally red (carne from the 2s orbital)? b. What fraction of the clay in this hybrid orbital was originally green (carne from a 2porbital)? c. Explain the name “ s(1/4)p(3/4) hybrid orbital” for each of the four orbitals. d. In fact, each of the four hybrid orbitals in the 109.5° set is called an sp3 -hybrid orbital.Explain the name “ sp3 -hybrid orbital.”
- What are all of the types of orbital overlaps that occur in the above structure. p-p overlap sp²-sp overlap s-sp² overlap sp²-sp² overlap s-sp overlap sp-sp overlap s-s overlap ---------- In cumulene, what are the C=C=C and H−C−H ideal bond angles, respectively?Enter the C=C=C bond angle followed by the H−C−H bond angle separated by a comma (no spaces, no º symbol required).each reagant must have 3 or less carbons . one image is the directions and one is the question.Assign Re and Si face to an SP2 hybridized carbon (C=O or C=C) Can you explain how to get it and provide a example?