Draw a tetrahedral representation of (S)-4,5-dimethyl-2-hexyne. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. ● .. H₂C-= CH3 CH₂ Q CH3 ? ChemDoodle

Draw a tetrahedral representation of (S)-4,5-dimethyl-2-hexyne. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. ● .. H₂C-= CH3 CH₂ Q CH3 ? ChemDoodle

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 21E

See similar textbooks

Related questions

Q: A possurgical patient weighs 185.0 1b and is prescribed a painkiller that has an administration…

A: First convert the given mass into pounds and then use the dosage amount to calculate the mg of…

Q: معمر Type of Reaction: H H₂N + [H] For the following molecule, draw the monomers a. What byproducts…

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: 4. a) Balance Ca(CN)2(a + b) What type of reaction is this? c) Is this a redox reaction, yes / no ?…

A: Answer:When solutions of two different substances are mixed and formation of precipitate takes…

Q: 4. Give the major organic product(s) for each of the following reactions. CH₂OH Nal Br CH3 CH₂S

A: Poor nucleophile and polar peotic solvent favour SN1 mechanismGood nucleophile and polar aprotic…

Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A: The addition of bromine to an alkene in a nonpolar solvent produces vicinal dibromo alkane.

Q: The amino acid cysteine has three ionizable groups with the indicated pKas values. Draw the shapes…

A: Given is amino acid .The name of amino acid is cysteine. It has three ionisable groups.

Q: H H CH₂CH3 H A CH₂CH3 H CH3CH₂- CH3 H H B CH3 CH3 CH3 H HU C CH3 CH3

A: Given are Newman projections for alkane.These constitutional isomers.

Q: 2+ Draw the molecular orbital (MO) electron diagram for the F2 molecular ion. Be sure your diagram…

Q: Draw a structural formula of the SS configuration of the compound shown below. S S

A: Given is organic compound.Given compound has two stereocenters.Both stereocenters have S,S…

Q: A 21.0 mL sample of a 0.433 M aqueous nitrous acid solution is titrated with a 0.442 M aqueous…

A: The concentration of the nitrous acid solution = 0.433 MThe volume of the nitrous acid solution =…

Q: KMnO4/mild OH- CHCl3/KOH

A: This problem is based on general organic chemistry reaction mechanism.Here, two reactions are given.…

Q: Draw the product of the E2 reaction shown below. Include the correct stereochemistry. Ignore any…

A: Given is E2 reaction.E2 stands for bimolecular elimination reaction.

Q: CH₂CH₂ Br: :OCH 3 A) B) 23. Which rate law is consistent with the reaction mechanism shown? C) D)…

A: The bimolecular nucleophilic substitution reaction is a concerted reaction that occurs in a single…

Q: The base protonation constant K₁ of lidocaine (C₁4H₂₁NONH) is 1.15 × 10¯⁹. 14 Calculate the pH of a…

A: The concentration of the lidocaine solution = 1.4 MThe base protonation constant of lidocaine = We…

Q: What is the major organic product of the following reaction? OI O III OIV OV I ỌCH3 IV AICI 3 OH II…

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: Problem 56 L 382 °C 10 s H j

A: 56.The given reaction is shown below.We have to draw the mechanism of this reaction.N.B.: According…

Q: Draw the product of this reaction with appropriate stereochemistry. Br₂ Click and drag to start…

Q: Choose the open-chain form for the following compound. НО HO- CH₂OH OH OH

A: The objective of the question is to draw the open-chain form of the given compound.The compound is a…

Q: 8. For the following molecule, draw the monomers *Hint* there are three different monomers a. What…

A: Addition polymers are formed by simple addition of monomers. There is no loss of small molecules…

Q: What is the % (v/v) concentration of a solution formed by mixing 5.06 mL of 2-propanol in enough…

A: The volume of 2-propanol = 5.06 mLThe final volume of the solution after the addition of water =…

Q: Mechanism: A reaction mechanism for the following reaction is shown below. H* CEN CEN: N-H || -C-OH…

A: In the given reaction a water molecule added to the nitrile group forming an imidic acid.The…

Q: Only typed answer otherwise leave it At 25°C the rate constant for the first-order decomposition…

A: The initial concentration of pesticide, [A0]=0.0314 MThe rate constant for the first-order…

Q: The acid dissociation constant Kof boric acid (H₂BO3) is 5.8 × 10 Calculate the pH of a 3.8M…

A: The concentration of boric acid = 3.8 MThe dissociation constant of boric acid = pH of the solution…

Q: 1. In carrying out a "density determination," assume that a small amount of liquid stays in the tip…

Q: Write the net ionic reaction for the following: a) Ca + Cu(NO3)2 → b) Cu + Mg(NO3)2 c) Mg + Zn(NO3)2…

A: Answer:When more reactive element is added to less reactive element then more reactive element…

Q: Complete the table below. Round each of your entries to 2 significant digits. You may assume the…

A: Answer:Any specie that loses H+ ion in its solution is called as Bronsted-Lowry acid and specie…

Q: 2. Provide a mechanism and the favored product(s) with the following reaction. Remember MeOH is…

A: The given reaction is shown below.We have to predict the major product of the reaction. We also have…

Q: 3) Draw the complete curved arrow mechanism and the major product. Be sure to check for carbocation…

A: Markovnikov's rule is applied to addition of unsymmetrical reagent to unsymmetrical…

Q: A student is examining a bacterium under the microscope. The E coll bacterial cell has a mass of…

Q: A solution is prepared at 25 °C that is initially 0.46M in dimethylamine ((CH3)₂NH), a weak base…

Q: reaction. swer KOH H₂O/EtOH

A: Given is organic reaction.In which reactant is ester.

Q: 3) Provide a curved-arrow mechanism: Br₂ CH₂OH tenor .Br

A: Given is organic reaction.In which reactant is cyclohexene.Thus is bromination reaction.

Q: A chemistry graduate student is given 125. mL of a 0.30M pyridine (CHN) solution. Pyridine is a weak…

A: The concentration of pyridine = 0.30 MThe Kb for pyridine = Mass of = ?

Q: Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to…

A: The molecules with the same molecular formula but different structures are known as isomers. If the…

Q: a solution with a density of 1.01 g/mL that is 1.11% HCl by mass Express your answer to three…

Q: 1. NaH 2.

A: Given is organic reaction.We have to predict the major product of the reaction.

Q: Draw the structural condensed form of 3-methyl-3-pentanol

A: Given is organic compound. The name of given compound is,3-methyl-3-pentanol.A condensed structural…

Q: A structural formula of a monosaccharide is shown below: HOH₂C- HO OH of H HO OH a. Classify this…

A: Given is monosaccharide molecule.Let's see answers and next step.

Q: Rank the following species in increasing terminal Se-O bond order (from lowest to highest). (H atoms…

A: Bond order is a fundamental concept in chemistry, influenced by the number of bonds and the…

Q: Draw the isomer of the compound below that can have all the groups equatorial with wedges and/or…

A: Given compound is cyclohexane derivative.We have to draw most stable conformation of this compound…

Q: Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate…

A: The molecules with the same molecular formula but different structures are known as isomers. If the…

Q: What is the product of the following reaction sequence? OH PCC (CH3)2NH [H₂SO4] -H₂O ?

A: Given is organic reaction. In which reactant is primary alcohol.

Q: 1. What volume of 1.00 M HNO2 when diluted to 100.00 mL in a volumetric flask would yield a 0.275 M…

A: The question is based on the concept of molarity. molarity is a method of expressing concentration…

Q: For the reaction 3 A + 4 B → 2 C + D, what is the magnitude of the rate of change for [B] when [D]…

A: The rate of the formation of the product or the rate of disappearance of the reactants is known as…

Q: 1. NaH 2. CO

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: A 24.0g sample of polyisoprene, which has a specific heat capacity of 1.880·J·g−1°C−1, is dropped…

A: This problem is based on Thermochemistry.Here, two substances are given one at high temperature and…

Q: what is the balanced equation of H2S + P4 = P4S2 + PH3

A: A chemical reaction follows the law of conservation of mass. According to the law of conservation of…

Q: Give the primary organic product for the reduction of the following compound.

A: Given is organic compound. The name of given compound is, 4-methylhexanal.It has aldehyde functional…

Q: CHO OCHO d a CH₂CH₂OH CH₂OH b Dess-Martin periodinane CH₂Cl2 CH₂CI с CH₂MgCl

A: The targeted compound synthesized using different types of regents. Including steps are reduction,…

Q: Н. -a) H3C CI CH3 b H3C. CH₂ H3C ОН CH3 c) Br- CH3 CI d) H3C. H3C- H3C- CH3 -ОН -CH3 CH3

A: The question is based on the concept of organic synthesis. We need to synthesize the product using…

Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

Draw a tetrahedral representation of (S)-4,5-dimethyl-2-hexyne.
O
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
• Include H atoms at chiral centers only.
• If a group is achiral, do not use wedged or hashed bonds on it.
+▾
II...
H₂C=
CH3
CH₂
CH3
?
ChemDoodle

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: Determine the tetrahedral representation structure of given molecule:

VIEW

Step 2: Explanation to write the name or structure of the molecules:

VIEW

Step 3: The structure of the molecule is:

VIEW

Solution

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 4 steps with 3 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

Part A. Using ChemDraw to Build Molecules. 1.) Draw t-butylcyclohexane C3 On ChemDraw, draw t-butylcyclohexane (see above). On Structure tab →Measurement > Generate all bond length (all bond angles, or dihedral angles). Locate the atoms desired. Note placing mouse on the bond also generates distances.Table shows up on the left side listing all the measured distances, angles and dihedral angles. a.) Measure the bond distance (with correct units): C1-C2 b.) Measure the bond angle (with correct units): C1-C2-C3 c.) Measure a dihedral angle, draw the molecule with the dihedral angle: d.) Define dihedral angle:
g) Reaction 1g pts] For 2-chloro-3-fluorocyclohexane, draw all possible stereoisomers, and identify their stereochemical relationships using the labels we used in class (E = enantiomers; D=Diastereomers; I = identical.) Make sure to label each chiral carbon in each compound with the correct R/S designation.
Draw the meso form of (1R,4R)-cycloheptane-1,4-diol Use the wedge/hash bond tools to indicate stereochemistry where it exists. Show stereochemistry in a meso compound.
Organic Chemistry, Ch.4, WS #2, Stereochemistry - Review of R&S configuration, Fischer Projections, Enantiomers, Diastereomers, Meso Compounds. 1. Assign R or S configuration to each stereocenter. (a) H₂C H₂C a H- H OH CH₂CH₂ - Br CH, (b) 2. For each Fischer Projection, assign R or S configuration. CH₂ CH₂CH₂ b. H₂N- H COOH + -H CH₂ C-OH (c) HTC OH CH₂OH C. Br- CH₂OH CI CHO CH
5. Draw the structure of (S)-1-bromo-1-chloropropane. Take care to indicate the three- dimensional stereochemistry properly. 6. How many chiral centers does the following compound contain? CH3 7. Label each chiral carbon in the molecule below as having R or S configuration. HO₂C H F. H3C H CH₂CH3
Draw the sold/dashed wedge structures (skeletal structure) for all stereoisomers of 3,4-dichloro 4-methylhexane. Label each structure with the proper R/S notation Label enantiomers and diastereomers
Draw a structural formula of the RR configuration of the compound shown below. Mastered R OH R AFFIL CH3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. Sn [F ? ChemDoodle Ⓡ
8. Identify the stereochemical relationship between the structural pairs shown below as (A) identical structures that are not meso; (B) identical structures that ARE meso; (C) structures that are enantiomers; or (D) structures that are diastereomers. a) b) H3C c) CH3 Br H. CH3 Br Br CH3 H. CI Holl H Cill Cl- CH3 Br H. CI CH3 HO. H. H3C Cl H3C- H- H. CH3 Cl a) b) c) 9. Identify the stereochemical relationship between the structural pairs shown below as (A) identical structures that are not meso; (B) identical structures that ARE meso; (C) structures that are enantiomers; or (D) structures that are diastereomers. a) b) c) CH2CH3 NH2 HO CH3 H3C. CH3 Cl HO H;C CH2CH3 F. F H;C. CI H H,N -CH3 CH3 NH2 H3C Br H2N C1 H3C CH3 CH3 H;CH,C- Cl F H. H Br CH,CH3 CH3 a) b) c)
Draw a structural formula of the S configuration of the compound shown below. CO2H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it. opy 8ste
A trisubstituted cyclohexane compound is given in its chair conformation. Draw the corresponding planar (overhead) representation, using wedge-and-dash bonds to indicate the substituent positions. Draw the planar cyclohexane. Clearly show stereochemistry. Select Draw Rings More Era //|の|/ CI H. Br CI F Br
5. Give the stereochemical relationship between each pair of isomers. Examples are same compound (meso), constitutional isomers, enantiomers, and diastereomers. H3C CH3 HO OH lll a. Но OH H Br CH3 b. C/ H3C CI H. ICH3 CH3 с. CH3 H. CH3 d. Но. H3C OH CH2OH Ho CH2OH Br e. Br H3C f. H CH3 H3C CH3
Predict the expected major product(s) of the following reaction sequence. ی ہیں میں قبر ہیں H 1. t-BuOK, t-BuOH 2. O3, CH2Cl2, -78 °C 3. MezS H OH OH + enantiomer H