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(a)
Interpretation:
Balanced equation for hydration of 1-butene has to be written.
Concept Introduction:
Addition of water molecule to an unsaturated bond present in hydrocarbon is known as hydration. During hydration, the unsaturated bond present is broken and a carbon‑hydrogen, carbon‑hydroxyl bond is formed.
General structure of
Alkene on hydration gives alcohol. As there is only one unsaturated bond present in alkene, only one molecule of water is consumed. The general equation for the hydration of alkene can be given as,
If the alkene is symmetrical only one product is formed. If the alkene is unsymmetrical, then the product is formed according the Markovnikov’s rule. According to this rule, in hydration reaction, the hydrogen atom gets attached to the carbon atom in the unsaturated bond which has more number of hydrogen atoms or less number of substituents.
(b)
Interpretation:
Balanced equation for hydration of 2-methyl-3-hexene has to be written.
Concept Introduction:
Refer part (a).
(c)
Interpretation:
Balanced equation for hydration of propene has to be written.
Concept Introduction:
Refer part (a).
(d)
Interpretation:
Balanced equation for hydration of 1,4-dichloro-2-butene has to be written.
Concept Introduction:
Refer part (a).
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Chapter 11 Solutions
General, Organic, and Biochemistry
- H2SO4 (cat.), H₂O 100 °C NH₂arrow_forwardX 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_forward
- 1A 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_forwardNonearrow_forwardIV. Show the detailed synthesis strategy for the following compounds. a. CH3CH2CH2CH2Br CH3CH2CCH2CH2CH3arrow_forward
- Do 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_forwardPredict and draw the product of the following organic reaction:arrow_forwardNonearrow_forward
- Redraw 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_forwardK 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_forward
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