AMoving to another question will save this response. Question 16 Which of the following names of organic compounds is most reactive toward electrophilic aromatic substitution relations? OA Florobenzene. O B. Aminobenzene. OC Benzyldehyde. OD. Toluene. OE. Nitrobenzene. A Moving to another question will save this response.

Click the "draw structure" button to launch the drawing utility. Write two different resonance forms for triphenylmethyl cation. Write the structure showing the positive charge at an ortho position. Write the structure showing the positive charge at a para position.

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Question 18 Which statement is incorrect as far as pyridine is concerned? O A. Aromatic. O B. it is planar. Oc.it is not conjugated. O D. The nitrogen is Sp2 hybridized. O E. It is cyclic. A Moving to another question will save this response. P Type here to search

The second question was incorrect. "The IUPAC nomenclature of benzene compounds primarily will use benzene as the root name. However, common names for substituted benzene compounds exist that use the base names from its derived compounds. The principal functional group will serve as the common root name." Would you mind trying again please? Thank you

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Question 8

Here is the chemical structure of methyl propanamide: H H. H H. H-C- C-C -N-C-H H. Decide whether each molecule in the table below is another mnolecule of methyl propanamide, a molecule of an isomer of methyl propanamide, or a molecule of an entirely different compound. molecule relationship to methyl propanamide NH-CH, (Choose one) another molecaule of methyl propanamide a molecule of an isomer of methyl propanamide a molecule of a different compound CH,-CH,-C=0 H H :o: H (Choose one) H-C H- H :0: H H H C-C (Choose one) H. H 回 山回

Organic Chemistry Маxwell Draw the organic and inorganic products for the following acid/base reaction. H .N. Н. 2 products H.

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