When 4-penten-2-one is reacted with aqueous NABH4 (sodium borohydride), the major substrate product will contain the following functional groups: alcohol only. alkene only. O ketone only. alkene & alcohol. alkene & ketone, since no reaction occurs under these conditions.

When 4-penten-2-one is reacted with aqueous NABH4 (sodium borohydride), the major substrate product will contain the following functional groups: alcohol only. alkene only. O ketone only. alkene & alcohol. alkene & ketone, since no reaction occurs under these conditions.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Related questions

Q: Describe how 1-ethylcyclohexanol can be prepared from cyclohexane. You can use any inorganic…

A: 3-methyl-1-phenyl-3-pentanol from benzene is shown below, Benzene is reacting with ethyl chloride in…

Q: Br2 NaN3 b) IBr (CH3),S=O EtONa, ETOH reflux CH;OH d) cat. H,SO4 ICI e) CH;OH H

A: The major product for all the given reactions is shown below with their appropriate stereochemistry…

Q: Although alcohol V gives a single alkene W when treated with POCI, and pyridine, three isomeric…

Q: 1. KMNO4, HO, Hа0, heat CH3 2. HС H,C- Product 2 ČH3

Q: Br

Q: What is the product for this reaction given the conditions specified: NAOCH, in CH,OH high…

Q: Reaction of this bicycloalkene with bromine in carbon tetrachloride gives a trans dibro- mide. In…

Q: Br. CH3ONA H

A: The conformer structure for given structure is shown below.

Q: ALKENE/ ALKYNE REAGENTS(S) AND MAJOR PRODUCTS(S) CONDITIONS ? OH

Q: Name each of the following cyclic sugars. (Consult Fig. 5-32 on p. 249 for the name of each sugar in…

A: Interpretation: The naming of given cyclic sugars is to be provided.

Q: Draw the organic product for each reaction sequence. Remember to include formal charges when…

A: Hi there! Since you have posted multiple questions, we will answer the first question for you. If…

Q: In each case below select the synthetic procedure's that could be used to carry out the…

A: The addition of oxygen atom is called oxidation or we can say that the removal of the hydrogen atom.…

Q: H. CH3 OH H, Can this alcohol be synthesized selectively by hydroboration-oxidation of an alkene? If…

A: Yes, the formation of organoborane through hydroboration of 1-methylcylopent-1-ene is shown below.

Q: Give the products when 1-methyl-2-deutero-cyclohexene is treated with the following reagents. Be…

A: The addition of H2 to the alkene forms the alkane, H2 adds in a 'syn' manner as follows: The…

Q: a. Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a…

Q: If 1-bromopentane is heated in acetone containing NaOH, what is the alkane produced? Draw and…

A: Here 1- bromopentane is heated in acetone containing NaOH. Here acetone is a polar aprotic solvent ,…

Q: 10. Classify the following alkenes as E or Z: CH3 Cilz0H • CH2 Br Citz0 NHz

A: The absolute configuration of alkenes are substituent dependent. The arrangement of substituents of…

Q: A.For the following reactions: Draw the products and identify the type of reaction. Identify which…

A: The given compound contains ether group as well as carboxylic acid group. Carboxylic acid group…

Q: R'R°CHOH-CR'R* R'R?C=CR*R* What should orientation of each substituent in reactant to convert it…

A: The given reactant is alcohol. The reaction given above is a dehydrating reaction. Here the alcohols…

Q: Which structures represent the two chair conformations of cis-1-tert-butyl-4-methylcyclohexane? O…

A: conformational isomers: The compound having the same molecular formula but which can be converted…

Q: 4) Write structures for products. Pay attention to stereochemistry OH L OH TsC1 Pyridine TsCl =+…

A: Addition reaction is a chemical reaction involving the addition of two or more molecules to form a…

Q: A.For the following reactions: Draw the products and identify the type of reaction. Identify which…

A: The given reaction is the reaction between acid and alcohol.

Q: Conversion of 2-methyl-2-butene into a tertiary alkyl halide. OBra. H0 O HBr, ROOR O Bra, ROOR HBr

Q: Draw the structure for an alkene that gives the following reaction product. 1. Hg(OАc)2, Н2О ?…

Q: suged to rearangenert 8) Dehydration of an unknown alcohol with concentrate@ H2SO4 results in the…

A: Note : Alcohols undergo acid catalyzed rearrangement. ( see below).

Q: 1. Illustrate and explain how the compound below can be used to produce different alkenes. wwwww

Q: When 4-penten-2-one is reacted with excess H2 (a lot of H2) with Pt, Pd or Ni metal, the major…

A: Addition of hydrogen in the presence of a metal catalyst such as Pt/Pd/Ni is known as hydrogenation…

Q: Complete these nucleophilic substitution reactions. In each reaction, show all electron pairs on…

A: SOLUTION: Step 1: The reaction of n-butyl bromide with sodium methoxide gives methyl propyl ether as…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. 1. Dry Et,0 at-60°…

A: A carbon centre can be made negatively charged by attaching a electropositive metal centre to it.…

Q: Draw the major organic products for this reaction. Show stereochemistry in your structures. Then in…

A: Osmium tetroxide OsO4 is used for dihydroxylation of alkenes. it gives always 1,2 diols (vicinal…

Q: Draw the major organic products for this reaction. Show stereochemistry in your structures. Then in…

A: Syn Hydroxylation of alkene :

Q: How many alkene products are possible in the following reaction? NaOEt - ? CH3 "CH3 H

A: The above reaction is E2 elimination. H and Chlorine are anti to each other prefers E2 elimination.

Q: Fill in the blanks: Br H₂C. CH₂ CH₂ The major product of the elimination of HBr from the above…

A: Given: Elimination reaction of .

Q: Ph Ph CH3 Ph CH3 The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with…

A: The mechanism for the first step that is nucleophilic addition is shown below,

Q: We haloalkane shown. CH,CH,C(CH;)2CH,CH,I

A: Haloalkane = CH3CH2C(CH3)2CH2CH2I Name of the haloalkane = ?

Q: Dihydroxylation of an alkene can be carried out with H2O2 in HCO2H. In this reaction,…

Q: + N₂ + H₂O CH3 Ph CH3 The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with…

Q: A dehydrohalogenation of an haloalkane yields The an alkene. Which of the two molecules completes…

Q: Complete the following nucleophilic substitution reactions. In each reaction, show all electron…

A: Given:

Q: MCPBA and Ag2O with O₂ at 350 °C are two ways of converting O alkyl halides Oalkenes Oethers…

Q: Ph Ph- CH3 Ph CH3 The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with…

A: To solve this problem we have to draw the arrow pushing mechanism of given step .

Q: name and draw the product/s formed from the reaction of 3-methylpent-2-ene: 1. with HBr 2. with…

Q: Page 8 in book Alcohols to hydroxynitriles - Example hello Construct a reaction scheme for…

A: The structure of propan-1-ol is as follows: The alcohol is oxidized into aldehyde and aldehyde…

Q: AICI3. + Ci-C-CH,CH3

A: The above reaction is an example of Fridel Craft's acylation. Where a acid chloride reacts with the…

Q: OH 1. Hg(OAc)2, H2O 2. NaBH4 CH3 .CH3 H3C Acid-catalyzed addition of water to an alkene yields an…

A: Given reaction is oxymercuration- demercuration reaction of alkene.

Q: 0. Complete the following reactions. Indicate stereochemistry where applicable *show HBr…

Q: Alkene X reacts with Br2 in H20 to give two major products. Neither of these products are chiral.…

Q: What alkene is needed to synthesize each 1,2-diol using (1) "OH in H,0? CH,CH,CH, но OH a. CH,CH,CH,…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. 1. Dry Et,0 at-60°…

A: Now a days umpolung strategy of making carbon atom a strong neucleophile by adding electropositive…

Question

When 4-penten-2-one is reacted with aqueous NaBH4 (sodium
borohydride), the major substrate product will contain the following
functional groups:
alcohol only.
alkene only.
ketone only.
alkene & alcohol.
alkene & ketone, since no reaction occurs under these conditions.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

When 4-penten-2-one is reacted with excess H2 (a lot of H2) with Pt, Pd or Ni metal, the major substrate product will contain the following functional groups: ketone only. alcohol only. alkene only. alkene & ketone, since no reaction occurs under these conditions. alkene and alcohol.
When 5-hexen-3-one is reacted with slightly less H2 than substrate, along with Pt, Pd or Ni metal, the major substrate product will contain the following functional groups: alkene & alcohol. alkene & ketone, since no reaction occurs under these conditions. alkene only. ketone only. alcohol only.
Draw the organic product(s) of the following reaction. CH3 H3C-C-CEC-H CH3 NaOC2Hs / CH5OH 1 eq. NANH2, NH3(1) CH;CH,CH,CH2-Br H-CEC-H H;C CH-Br H3C 1 eq. NaNH2, NH3() H3C-CEC-H
МЕСНANISMS 1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed opening of the epoxide ring to form two different products. > Using ethanol as the solvent and an appropriate acid, show the steps in the acid catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). > Using ethanol as the solvent and an appropriate base, show the steps in the base- catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). 1,2-epoxy-1-methylcyclopentane CH3
(a) 2-methyl-2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. AAVIL ? ChemDoodleⓇ Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 01. BH3; 2. H₂O2, NaOH OsO4, H₂O2 On n [ ]#
CH3 CH3 CH3 CH;=ĊCH,CHCH;OH H2SO4, H3C H3C Referring to the above reaction: 1. Which atom does the H2SO4 first remove? 2. Identify the reaction if it's hydrogenation, hydrohalogenation, etc. 3. Propose a mechanism for the reaction, using the arrow formalism to indicate the flow of electrons.
3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOH
Q17. Compound 1 can undergo an intramolecular reaction to give cyclic product 2. Using curly arrows, show the mechanism of this reaction – note that the mechanism involves more than one elemental step - and draw the structure of 2; chemical formula is provided as guidance. H,N. CsHgNO + CH;OH 2
Draw the organic products formed when cyclopentene is treated with each reagent. With some reagents, no reactionoccurs.a. H2 + Pd-Cb. H2 + Lindlar catalystc. Na, NH3d. CH3CO3He. [1] CH3CO3H; [2] H2O, HO–f. [1] OsO4 + NMO; [2] NaHSO3, H2Og. KMnO4, H2O, HO–h. [1] LiAlH4; [2] H2Oi. [1] O3; [2] CH3SCH3j. (CH3)3COOH, Ti[OCH(CH3)2]4, (–)-DETk. mCPBAl. Product in (k); then [1] LiAlH4; [2] H2O
Consider a reaction where cis-but-2-ene is treated with sO followed by NaHSO/H, O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
The major product formed by addition of HBr to (CH3)₂C=CH-CH=C(CH3)₂ is the same at low and high temperature. Part 1 out of 2 Draw the structure of the major product. draw structure...
Q17. Compound 1 can undergo an intramolecular reaction to give cyclic product 2. Using curly arrows, show the mechanism of this reaction – note that the mechanism involves more than one elemental step - and draw the structure of 2; chemical formula is provided as guidance. H2N. C5H9NO CH3OH 2