Please correct answer and don't used hand raiting Current Attempt in ProgressRank the following compounds from lowest to highest heat of hydrogenation.ааааOV<<<OV<<<OK<<

given hydrocarbon is a cyclic alkene.rank the lowest to highest heat of hydrogenation. it can be…

Answered: Current Attempt in Progress Rank the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter12: Chirality

Section: Chapter Questions

Problem 25CTQ

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CH3 to Br- -H + Nal • product; Sy2 product of the reaction is : Аcetone H- -CH3 CH2 – CH3 CH3 CH3 CH3 CH3 it it -H H- -CH3 (d) -CH3 -H- (а) H• (Ъ) H- -CH3 -CH3 (с) H- CH -H- ČH2 – CH3 ČH2 – CH3 CH2 – CH3 CH2- CH3 2.
E!!- Alkyl halide: Same as SNI Bay / NU! Same as SN' in presence of heat -OH H₂say
what is the major organic product for the reaction shown below?
Fill in the fields (reagent or products) left blank in the reaction below.
please help with attached
please helpppp.
What is an appropriate stepwise synthesis for 1-pentanol from butanal? NABH4/CH3OH; PBr3; Mg/ether; H;C , H3O* CH3 NABH4/CH3OH; PBr3; Mg/ether; ;H30* H' H. NaBH4/CH3OH; Mg/ether; ;H30* NABH4/CH3OH; Mg/ether; H3C , H3O* CH3 NABH4; PB13; Mg/ether; H' H.
:&&/&&:&:&&:&&
O (1) H20, H*; (2) Jones reagent (1) H20, H*; (2) PCC, CH2CI2 (1) conc. H2SO4: (2) Jones reagent O (1) H20, H*; (2) Tollens reagent (1) conc. H2SO4: (2) PCC, CH2CI2 O (1) conc. H2SO4: (2) Tollens reagent
Which of the following carbocations can rearrange to a more stable ion? Propose structures for the likely rearrangement products.
ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamine
Provide reasonable IUPAC names for 4 of following structures.

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Current Attempt in Progress Rank the following compounds from lowest to highest heat of hydrogenation. аааа OV<<< OV<<< OK<<