Select the correct IUPAC name for the following branched chain alkane. CH3 CH3 | CH3CHCH₂CH₂CH2CHCHCH3 CH3CH₂CH₂1 - CH3 -CH,CH,CHCH,CH3 CH₂CH3 7,10-diethyl-2,6-dimethyl-6-(1-methylethyl)dodecane 10-ethyl-2,7-dimethyl-6-(1-methylbutyl)-7-propyldodecane 10-ethyl-2,7-dimethyl-6-(1-methylethyl)-7-propyldodecane 6,9-diethyl-4,6-dimethyl-5-(4-methylpentyl)undecane

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Q: Which of these species is aromatic? IZ: 0: II IZ: III 2:00: 0 IV un V

A:

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Q: Are the following cations aromatic? Draw resonance structures to figure it out! Compound Resonance…

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Q: 4. Give the IUPAC names of the following compounds.

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Q: Give the name for this molecule: CH3CH₂CH₂ N-H H

A: The name for the given compound.

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Q: Give only typing answer with explanation and conclusion Draw the resonance structures for…

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Q: identify the functional groups present in the structure below. HN- N Functional Groups a. alkene b.…

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Q: Br Br

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Q: 4)How many covalent bonds can you count looking at this molecule? O-C=O

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Q: Which species will be largest? Sn-1 Sn+ In-1 In+

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Q: How many double bonds are present in the "best" resonance structure of the iodate ion?

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Q: How many kinds of chemically non-equivalent hydrogens are there in each of the following compounds?…

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Q: For the following molecules classify them as aromatic, antiaromatic, or nonaromatic. ||

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Q: Which of the following molecules is the most polar? CH31 BF3 NH3 N₂

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Q: What is the IUPAC name for the following compound?

A: The given compound is a thioether. The IUPAC name of a thioether is written as follows:

Q: Give  IUPAC  name

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A:

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A: These can be calculated base on Woodward Fieser rules.

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Q: Draw the line angle and condensed structural formula for the following species. a. Hexanamide b.…

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Q: What is an azeotropic mixture? Can they be separated using simple or fractional distillation? Can…

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Q: Label the following structures as either aromatic or non-aromatic. Also provide clear explanation…

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Q: Aniline can be formed by the hydrogenation of nitrobenzene. True or False True False

A: Anniline can be formed by hydrogenation of nutrobenzene.

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Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.