(a)
Interpretation:
The compound 1-pentene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
(b)
Interpretation:
The compound 2-pentene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
(c)
Interpretation:
The compound 1-chloropropene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
(d)
Interpretation:
The compound 2-chloropropene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
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Chapter 15 Solutions
CHEMISTRY:MOLECULAR...V.2 W/ACCESS
- X Draw the major products of the elimination reaction below. If elimination would not occur at a significant rate, check the box under the drawing area instead. ది www. Cl + OH Elimination will not occur at a significant rate. Click and drag to start drawing a structure.arrow_forwardNonearrow_forward1A H 2A Li Be Use the References to access important values if needed for this question. 8A 3A 4A 5A 6A 7A He B C N O F Ne Na Mg 3B 4B 5B 6B 7B 8B-1B 2B Al Si P 1B 2B Al Si P S Cl Ar K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe * Cs Ba La Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn Fr Ra Ac Rf Ha ****** Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr Analyze the following reaction by looking at the electron configurations given below each box. Put a number and a symbol in each box to show the number and kind of the corresponding atom or ion. Use the smallest integers possible. cation anion + + Shell 1: 2 Shell 2: 8 Shell 3: 1 Shell 1 : 2 Shell 2 : 6 Shell 1 : 2 Shell 2: 8 Shell 1: 2 Shell 2: 8arrow_forward
- Nonearrow_forwardIV. Show the detailed synthesis strategy for the following compounds. a. CH3CH2CH2CH2Br CH3CH2CCH2CH2CH3arrow_forwardDo the electrons on the OH participate in resonance with the ring through a p orbital? How many pi electrons are in the ring, 4 (from the two double bonds) or 6 (including the electrons on the O)?arrow_forward
- Predict and draw the product of the following organic reaction:arrow_forwardNonearrow_forwardRedraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ Parrow_forward
- K m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11arrow_forwardNonearrow_forwardPlease provide a mechanism of synthesis 1,4-diaminobenzene, start from a benzene ring.arrow_forward
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