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- O REPRESENTATIONS OF ORGANIC MOLECULES Identifying bonds with restricted rotation Examine the molecule below. Highlight all bonds that cannot rotate freely with respect to the rest of the molecule. IIIReview TopicS TReferences Click on all of the atoms that make up the largest coplanar unit in the molecule below. H H H. H' H. ннThe Lewis structure of an organic compound is shown below. Determine the orbitals used in bonding, as well as the number of sigma and pi bonds. 1ペー= 10 H 5. :N. 11 Total sigma bonds: [Select ] Total pi bonds: [Select] Write "none" if no orbital of that type is used to bond. Unhybridizedorbital used to Hybridized orbital used to Atom bond bond H. [ Select ] [Select] [ Select ] [ Select] N C #2 [ Select] [ Select] [ Select ] [ Select ]
- Write the molecular diagram for the following molecules O2 H2 Write their molecular electronic configuration. State the order for each molecule aboveNumber of Molecule valence electrons Formal Charge Electron-Group Geometry Molecular Geometry Resonance COSe C: C: Select one ... C: Select one.. Select one .. SH412 S: S: Select one .. S: Select one .. Select one ... SeHĄBr2 Se: Se: Select one... Se: Select one ... Select one ... AtGeN Ge: Ge: Select one ... Ge: Select one ... Select one ... CIGEP Ge: Ge: Select one... Ge: Select one ... Select one ... V 10000A. Classify the following hypothetical molecules as polar or non-polar. Note: Number 5 item is not a hypothetical molecule. (The number of valence electrons are given in parenthesis.) Explain your answer in terms of: (a) Lewis structure (b) Molecular geometry (c) Symmetry (symmetrical or asymmetrical) (d) Dipole moment (descriptive) Molecule/ Ion (No. of Valence Non-polar electron) 2. MJ2 (M=8, J=7) Polar or Explanation
- (please give clear handwritten answer) Draw a complete molecular orbital diagram for LiF. Explain that Energy levels of the atomic orbitals and what kind of character the bonding and antibonding orbitals display.The energy penalty that is accrued when large groups in a molecule are forced into proximity to one another is known as strain Provide a systematic name for the compound shown below. AIf A H;º is a positive number then that molecule has less chemical potential energy stored in its' bonds than the elemnets it was formed from. that molecule has more chemical potential energy stored in its' bonds than the elemnets it was formed from. that molecule has the same amount of chemical potential energy stored in its' bonds as the elemnets it was formed from.
- Number of Molecule valence electrons Formal Charge Electron-Group Geometry Molecular Geometry Resonance AIH2ATCI- Al: Al: Select one.. Al: Select one .. Select one ... AIHAT,Br Al: Al: Select one ... Al: Select one ... Select one ... FSIAS Si: Si: Select one .. Si: Select one ... Select one .. PHATCI P: P: Select one ... P: Select one.. Select one .. PCIFI P: P: Select one ... P: Select one ... Select one ... vDescribe the AXE labeling system for VSEPR in detail. What does each letter stand for? For each of the electron and molecular geometries, assign the AXE notation.In a sample of bonds in the position. (Note: Remember that iodine () is larger and more likely to contribute to steric strain in the molecule.) iodocyclohexane (CH), one would expect to find most of the C-I O equatorial O trigonal pyramidal O tetrahedral Oplanar O axial Question 7 The molecule aniline is pictured here. Which of the following words could be used to describe an essential feature of aniline to someone who is familiar with chemistry, but not with this molecule? O aromatic O heterocycle O non-cyclic fused-ring system O alkane NH₂